CN1384861A - Fluorochemical adhesive material and layered product obtained with the same - Google Patents
Fluorochemical adhesive material and layered product obtained with the same Download PDFInfo
- Publication number
- CN1384861A CN1384861A CN00815080A CN00815080A CN1384861A CN 1384861 A CN1384861 A CN 1384861A CN 00815080 A CN00815080 A CN 00815080A CN 00815080 A CN00815080 A CN 00815080A CN 1384861 A CN1384861 A CN 1384861A
- Authority
- CN
- China
- Prior art keywords
- layer
- fluorine
- multilayer body
- adhesive material
- containing adhesive
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000463 material Substances 0.000 title claims abstract description 211
- 239000000853 adhesive Substances 0.000 title claims abstract description 133
- 230000001070 adhesive effect Effects 0.000 title claims abstract description 133
- 239000000126 substance Substances 0.000 claims abstract description 115
- XUCNUKMRBVNAPB-UHFFFAOYSA-N fluoroethene Chemical group FC=C XUCNUKMRBVNAPB-UHFFFAOYSA-N 0.000 claims abstract description 79
- 125000005587 carbonate group Chemical group 0.000 claims abstract description 55
- 229920000642 polymer Polymers 0.000 claims abstract description 50
- 150000004820 halides Chemical group 0.000 claims abstract description 35
- 239000011521 glass Substances 0.000 claims abstract description 20
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 13
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims abstract description 5
- 239000010410 layer Substances 0.000 claims description 203
- 229910052731 fluorine Inorganic materials 0.000 claims description 132
- 239000011737 fluorine Substances 0.000 claims description 124
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims description 122
- 238000000034 method Methods 0.000 claims description 64
- 238000000465 moulding Methods 0.000 claims description 57
- 230000015572 biosynthetic process Effects 0.000 claims description 56
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 43
- BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 claims description 42
- 239000002253 acid Substances 0.000 claims description 36
- 239000000178 monomer Substances 0.000 claims description 31
- 125000000524 functional group Chemical group 0.000 claims description 28
- 239000011368 organic material Substances 0.000 claims description 26
- -1 alkyl vinyl ether) class Chemical class 0.000 claims description 23
- 238000003475 lamination Methods 0.000 claims description 23
- 229910010272 inorganic material Inorganic materials 0.000 claims description 20
- 239000011147 inorganic material Substances 0.000 claims description 20
- 230000007704 transition Effects 0.000 claims description 20
- 125000004429 atom Chemical group 0.000 claims description 18
- 238000001125 extrusion Methods 0.000 claims description 18
- 239000000446 fuel Substances 0.000 claims description 17
- 238000004519 manufacturing process Methods 0.000 claims description 14
- 238000009826 distribution Methods 0.000 claims description 13
- 229920002647 polyamide Polymers 0.000 claims description 13
- 238000002844 melting Methods 0.000 claims description 10
- 230000008018 melting Effects 0.000 claims description 10
- 229920005992 thermoplastic resin Polymers 0.000 claims description 10
- 238000007334 copolymerization reaction Methods 0.000 claims description 9
- 239000007769 metal material Substances 0.000 claims description 9
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000002828 fuel tank Substances 0.000 claims description 7
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 claims description 6
- 239000002861 polymer material Substances 0.000 claims description 6
- 235000014347 soups Nutrition 0.000 claims description 6
- 229920000728 polyester Polymers 0.000 claims description 5
- 125000004185 ester group Chemical group 0.000 claims description 4
- 229920000515 polycarbonate Polymers 0.000 claims description 4
- 239000004417 polycarbonate Substances 0.000 claims description 4
- 229920000098 polyolefin Polymers 0.000 claims description 4
- 229920000219 Ethylene vinyl alcohol Polymers 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 229910052801 chlorine Inorganic materials 0.000 claims description 3
- 125000003700 epoxy group Chemical group 0.000 claims description 3
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 3
- QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 claims description 3
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 3
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical group NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 claims description 2
- 150000007942 carboxylates Chemical group 0.000 claims description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 150000003949 imides Chemical class 0.000 claims description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 claims description 2
- 239000011241 protective layer Substances 0.000 claims description 2
- 125000001273 sulfonato group Chemical class [O-]S(*)(=O)=O 0.000 claims 2
- 125000003262 carboxylic acid ester group Chemical group [H]C([H])([*:2])OC(=O)C([H])([H])[*:1] 0.000 claims 1
- 229920001038 ethylene copolymer Polymers 0.000 claims 1
- 239000011118 polyvinyl acetate Substances 0.000 claims 1
- 239000004800 polyvinyl chloride Substances 0.000 claims 1
- 229920002313 fluoropolymer Polymers 0.000 abstract description 82
- 239000004811 fluoropolymer Substances 0.000 abstract description 82
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract description 73
- 229920005989 resin Polymers 0.000 abstract description 42
- 239000011347 resin Substances 0.000 abstract description 42
- 239000002904 solvent Substances 0.000 abstract description 28
- 229910052751 metal Inorganic materials 0.000 abstract description 18
- 239000002184 metal Substances 0.000 abstract description 18
- 150000002739 metals Chemical class 0.000 abstract description 2
- 239000000758 substrate Substances 0.000 abstract 1
- 239000010408 film Substances 0.000 description 55
- 238000003786 synthesis reaction Methods 0.000 description 49
- 150000001408 amides Chemical class 0.000 description 31
- 238000006116 polymerization reaction Methods 0.000 description 31
- 239000011236 particulate material Substances 0.000 description 29
- 239000003153 chemical reaction reagent Substances 0.000 description 25
- 239000003795 chemical substances by application Substances 0.000 description 24
- 239000000203 mixture Substances 0.000 description 23
- 238000009740 moulding (composite fabrication) Methods 0.000 description 23
- 239000000843 powder Substances 0.000 description 23
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 18
- 239000004567 concrete Substances 0.000 description 18
- 239000005977 Ethylene Substances 0.000 description 17
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 16
- 229910000831 Steel Inorganic materials 0.000 description 16
- 229920001577 copolymer Polymers 0.000 description 16
- 239000010959 steel Substances 0.000 description 16
- 239000002313 adhesive film Substances 0.000 description 13
- 229910052782 aluminium Inorganic materials 0.000 description 13
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 13
- 229920000840 ethylene tetrafluoroethylene copolymer Polymers 0.000 description 13
- 238000010438 heat treatment Methods 0.000 description 13
- 229910045601 alloy Inorganic materials 0.000 description 12
- 239000000956 alloy Substances 0.000 description 12
- 150000001875 compounds Chemical class 0.000 description 12
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 150000001265 acyl fluorides Chemical class 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 11
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- 229920002981 polyvinylidene fluoride Polymers 0.000 description 10
- 238000012545 processing Methods 0.000 description 10
- 239000000654 additive Substances 0.000 description 9
- 239000011248 coating agent Substances 0.000 description 9
- 238000000576 coating method Methods 0.000 description 9
- BEQKKZICTDFVMG-UHFFFAOYSA-N 1,2,3,4,6-pentaoxepane-5,7-dione Chemical compound O=C1OOOOC(=O)O1 BEQKKZICTDFVMG-UHFFFAOYSA-N 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- 239000011230 binding agent Substances 0.000 description 7
- 239000006185 dispersion Substances 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000007789 gas Substances 0.000 description 7
- 229930195733 hydrocarbon Natural products 0.000 description 7
- 230000008569 process Effects 0.000 description 7
- 239000000243 solution Substances 0.000 description 7
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 6
- 239000004411 aluminium Substances 0.000 description 6
- 238000011156 evaluation Methods 0.000 description 6
- 150000004978 peroxycarbonates Chemical class 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 6
- 239000004033 plastic Substances 0.000 description 6
- 239000004593 Epoxy Substances 0.000 description 5
- 239000004952 Polyamide Substances 0.000 description 5
- 230000001464 adherent effect Effects 0.000 description 5
- 229910052799 carbon Inorganic materials 0.000 description 5
- 238000006243 chemical reaction Methods 0.000 description 5
- 238000001035 drying Methods 0.000 description 5
- 150000002221 fluorine Chemical class 0.000 description 5
- HCDGVLDPFQMKDK-UHFFFAOYSA-N hexafluoropropylene Chemical group FC(F)=C(F)C(F)(F)F HCDGVLDPFQMKDK-UHFFFAOYSA-N 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 239000003960 organic solvent Substances 0.000 description 5
- 239000002245 particle Substances 0.000 description 5
- 238000011160 research Methods 0.000 description 5
- 238000003756 stirring Methods 0.000 description 5
- 238000007725 thermal activation Methods 0.000 description 5
- 238000011282 treatment Methods 0.000 description 5
- 238000005406 washing Methods 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 229910018505 Ni—Mg Inorganic materials 0.000 description 4
- 239000004721 Polyphenylene oxide Substances 0.000 description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 4
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 4
- 239000006096 absorbing agent Substances 0.000 description 4
- 239000002390 adhesive tape Substances 0.000 description 4
- 239000004568 cement Substances 0.000 description 4
- 239000010949 copper Substances 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 230000007797 corrosion Effects 0.000 description 4
- 238000005260 corrosion Methods 0.000 description 4
- 230000007812 deficiency Effects 0.000 description 4
- 230000002950 deficient Effects 0.000 description 4
- 238000006073 displacement reaction Methods 0.000 description 4
- 230000002349 favourable effect Effects 0.000 description 4
- 238000005187 foaming Methods 0.000 description 4
- 239000011229 interlayer Substances 0.000 description 4
- 229910044991 metal oxide Inorganic materials 0.000 description 4
- 150000004706 metal oxides Chemical class 0.000 description 4
- 229910052759 nickel Inorganic materials 0.000 description 4
- 239000000049 pigment Substances 0.000 description 4
- 229920006380 polyphenylene oxide Polymers 0.000 description 4
- 229930195734 saturated hydrocarbon Natural products 0.000 description 4
- 229910052710 silicon Inorganic materials 0.000 description 4
- 239000010703 silicon Substances 0.000 description 4
- 229910001220 stainless steel Inorganic materials 0.000 description 4
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- 239000012745 toughening agent Substances 0.000 description 4
- 229910000838 Al alloy Inorganic materials 0.000 description 3
- JHWNWJKBPDFINM-UHFFFAOYSA-N Laurolactam Chemical compound O=C1CCCCCCCCCCCN1 JHWNWJKBPDFINM-UHFFFAOYSA-N 0.000 description 3
- 229920000299 Nylon 12 Polymers 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 238000000862 absorption spectrum Methods 0.000 description 3
- 238000004026 adhesive bonding Methods 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- KRVSOGSZCMJSLX-UHFFFAOYSA-L chromic acid Substances O[Cr](O)(=O)=O KRVSOGSZCMJSLX-UHFFFAOYSA-L 0.000 description 3
- 239000011651 chromium Substances 0.000 description 3
- 238000010411 cooking Methods 0.000 description 3
- 210000003298 dental enamel Anatomy 0.000 description 3
- 238000009713 electroplating Methods 0.000 description 3
- AWJWCTOOIBYHON-UHFFFAOYSA-N furo[3,4-b]pyrazine-5,7-dione Chemical compound C1=CN=C2C(=O)OC(=O)C2=N1 AWJWCTOOIBYHON-UHFFFAOYSA-N 0.000 description 3
- 230000004927 fusion Effects 0.000 description 3
- 238000007731 hot pressing Methods 0.000 description 3
- 239000004973 liquid crystal related substance Substances 0.000 description 3
- BCCOBQSFUDVTJQ-UHFFFAOYSA-N octafluorocyclobutane Chemical compound FC1(F)C(F)(F)C(F)(F)C1(F)F BCCOBQSFUDVTJQ-UHFFFAOYSA-N 0.000 description 3
- 235000019407 octafluorocyclobutane Nutrition 0.000 description 3
- 230000000379 polymerizing effect Effects 0.000 description 3
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- 239000011734 sodium Substances 0.000 description 3
- 239000007858 starting material Substances 0.000 description 3
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- 229920003002 synthetic resin Polymers 0.000 description 3
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- BLTXWCKMNMYXEA-UHFFFAOYSA-N 1,1,2-trifluoro-2-(trifluoromethoxy)ethene Chemical compound FC(F)=C(F)OC(F)(F)F BLTXWCKMNMYXEA-UHFFFAOYSA-N 0.000 description 2
- 229910018134 Al-Mg Inorganic materials 0.000 description 2
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- 229910000906 Bronze Inorganic materials 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
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- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
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- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 description 1
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- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 1
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- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2369/00—Polycarbonates
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/31536—Including interfacial reaction product of adjacent layers
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/31504—Composite [nonstructural laminate]
- Y10T428/3154—Of fluorinated addition polymer from unsaturated monomers
- Y10T428/31544—Addition polymer is perhalogenated
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- Engineering & Computer Science (AREA)
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- Laminated Bodies (AREA)
- Adhesives Or Adhesive Processes (AREA)
Abstract
A fluorochemical adhesive material which comprises a fluoroethylene polymer which has a carbonate group and/or carbonyl halide group at a polymer chain end or in a side chain and in which the total number of the carbonate and carbonyl halide groups is less than 150 per 1x10<6> carbon atoms constituting the main chain. The material tenaciously adheres directly to substrates such as metals, glasses, and resins while retaining excellent properties inherent in the fluoropolymer, such as chemical resistance, solvent resistance, weatherability, and unsusceptibility to fouling.
Description
Invention field
The present invention relates to a kind of can with the fluorine-containing adhesive material of organic materialss such as various synthetic resins or multiple material good bond such as inorganic materials such as metal, glass.Further relate to multilayer body, moulded products that uses fluorine-containing adhesive material and the manufacture method that is used to obtain this moulded products.
Correlation technique
In the past, fluoropolymer has good thermotolerance, resistance to chemical reagents, weathering resistance, surface property (low frictional properties etc.), electrical insulating property owing to it, and is used in the various uses.Particularly aspect solvent resistance, fluoropolymer is insoluble to most of solvent, and soaking into and permeating of solvent also had very high tolerance, therefore is widely used in the transfer lime of fuel, coating or soup or the liner of pipe.
On the other hand, in general, the physical strength of fluoropolymer and dimensional stability deficiency, and cost an arm and a leg.
Therefore, in order to bring into play the advantage of fluoropolymer to greatest extent, and make its shortcoming, carrying out the research of various compoundization such as bonding, laminationization about fluoropolymer and other organic materialss or inorganic materials for minimum.
But, generally be difficult to make fluoropolymer and other materials directly bonding, even attempt to adopt methods such as heat fusing to carry out bonding, bonding strength is also abundant inadequately, even when obtaining bonding force to a certain degree, bonding force is also often inhomogeneous easily, thereby makes adhesion reliability insufficient.
As making fluoropolymer and other materials adherent method, having of main research is following several:
1. adopt methods such as sandblasting, make the surface physics roughening of the moulding product that one or both materials make method,
The moulding product that fluoropolymer is made carry out surface-treated methods such as sodium etching, Cement Composite Treated by Plasma, photochemical treatment,
3. with tackiness agent adherent method, above-mentioned the 1st, the 2nd method needs treatment process, and complex procedures, and productivity is poor.In addition, the kind of material and the shape of moulded products are limited, the outward appearance of the multilayer body of acquisition also go wrong easily (painted and scratch).Further, even carry out these processing, also can't see bonding force and significantly improve.
Various researchs have also been carried out about the tackiness agent in above-mentioned the 3rd method.But because the bonding force deficiency of general employed hydrocarbon system tackiness agent, and use in the multilayer body of this tackiness agent, the thermotolerance of binder layer, resistance to chemical reagents, water tolerance deficiency, therefore, bonding force is along with temperature variation or environmental change and can not get keeping, thereby cause lacking reliability, and, be difficult to give the above-mentioned good characteristic that fluoropolymer has to multilayer body.
On the other hand, present tackiness agent or the binder composition that is carrying out forming about the fluoropolymer that those is had functional group is used for adherent research.
For example, will have carboxyl such as maleic anhydride or vinyltrimethoxy silane etc. relevant in tackiness agent, using, carboxylic anhydride residue, epoxy group(ing), the hydrocarbon system of water-disintegrable silyl is monomer-grafted be aggregated in the fluoropolymer and the report of the fluoropolymer that forms (for example the spy opens flat 7-18035 number, Te Kaiping 7-25952 number, Te Kaiping 7-25954 number, Te Kaiping 7-173230 number, Te Kaiping 7-173446 number, wait communique Te Kaiping 7-173447 number), the adhesive composition that fluorinated copolymer that obtains about the hydrocarbon system monomer that will contain functional group such as hydroxyalkyl vinyl ether and tetrafluoroethylene or a chlorotrifluoroethylene copolymerization and isocyanate-based solidifying agent are formed is used for vinylchlorid and report (for example the spy opens flat 7-228848 communique) through the tackiness agent of the ETFE of Corona discharge Treatment (ethylene/tetrafluoroethylene polymkeric substance).
These uses contain the monomer-grafted polymerization of hydrocarbon system functional group or the tackiness agent or the binder composition of the fluoropolymer that copolymerization forms, the thermotolerance of itself is not fully improved, cause decomposition and foaming etc. when at high temperature using, bonding strength is reduced, and peel off with painted.In addition, when stating the spy in the use and opening the binder composition of putting down in writing in the flat 7-228848 communique, fluoro-resin (ETFE) must carry out Corona discharge Treatment in advance, and is uneconomical.
And, there is report to claim, will contain the perfluorovinyl sulfide ether compound and the fluorochemical monomer copolymerization of carboxylic acid or derivatives thereof, the fluoropolymer with functional group that obtains is used for tackiness agent or binder composition.U.S. Patent No. 4,916 disclosedly in No. 020 specification sheets is to make the synthetic multilayer body that have the fluoropolymer of functional group and use this fluoropolymer of copolymerization such as perfluoroalkyl vinyl ether with carboxylic acid group's or derivatives thereof and tetrafluoroethylene.
But, this multilayer body multilayer body that to be above-mentioned fluoropolymer with carboxylic acid group etc. form by resin of binding property such as Resins, epoxy or urethane resin and metal or other material laminate, rather than it is directly bonding with metal, glass or other resin, so exist in use, thermotolerance, the resistance to chemical reagents of Resins, epoxy or urethane resin etc., the problem of solvent resistance.And, do not describe making fluoropolymer be directly bonded to method on metal, glass or other resin in this report clearly.
Brief summary of the invention
The objective of the invention is to, solve above-mentioned problem in the past, provide a kind of and keep characteristics such as good resistance to chemical reagents, solvent resistance, weathering resistance, didirtresistance and non-binding property that fluoropolymer has constant the time, also give fluorine-containing adhesive material, the multilayer body of using this fluorine-containing adhesive material and moulded products with direct strong bond power of material such as metal, glass or resins.Further, the present invention also aims to, provide a kind of heating and melting adherent method that particularly adopts can be with the fluorine-containing adhesive material of above-mentioned materials good bond and by its multilayer body that constitutes.
Fluorine-containing adhesive material of the present invention is that number is in carbonate group in the certain limit and/or the vinyl fluoride polymkeric substance that contains of acid halide group constitutes by having on polymer chain end or side chain.Present inventors find, by in containing the vinyl fluoride polymkeric substance, introducing carbonate group or acid halide group, even do not carry out those surface treatments that fluoro-resin carries out usually or the processing of lining resin of binding property (undercoat etc.) etc. when bonding, fluorine-containing adhesive material also can demonstrate the surprising powerful bonding force to synthetic resins, metal, glass or other material.
Further, present inventors also find, the carbonate group by will containing the vinyl fluoride polymkeric substance and the total number of acid halide group limit within the specific limits, carbonate group or acid halide group can be followed bonding operation and the inferior limit that is suppressed at of the caused gas of chemical transformation takes place, can improve bonding force thus.
In addition, present inventors also find, by selecting specific vinyl fluoride polymkeric substance and compatibility material and specific condition of molding, the moulded products that can obtain to keep the multilayer body of strong bond power and use this multilayer body of containing.
Detailed description of the invention
Fluorine-containing adhesive material of the present invention is to be made of the vinyl fluoride polymkeric substance that contains that has carbonate group and/or acid halide group on polymer chain end or side chain, when having carbonate group, the number of this carbonate group is with respect to the backbone c atoms that contains the vinyl fluoride polymkeric substance several 1 * 10
6Individual is 150 of less thaies, and when having acid halide group, the number of this acid halide group is with respect to the backbone c atoms that contains the vinyl fluoride polymkeric substance several 1 * 10
6Individual is 150 of less thaies, when have carbonate group and acid halide group the two the time, the total number of these groups is with respect to the backbone c atoms that contains the vinyl fluoride polymkeric substance several 1 * 10
6Individual is 150 of less thaies.Among the present invention, when being acid halide group separately, its number is with respect to the backbone c atoms that contains the vinyl fluoride polymkeric substance several 1 * 10
6Individual can less than 100.In addition, in the following description, carbonate group and/or acid halide group are referred to as " containing the carbonyl functional group ".
Fluorine-containing adhesive material of the present invention is to contain carbonyl functional group and this number that contains the carbonyl functional group with respect to backbone c atoms several 1 * 10 by having on polymer chain end or side chain
6The individual vinyl fluoride polymkeric substance that contains for 150 of less thaies constitutes.The number that contains the carbonyl functional group is at 150 when above, fluorine-containing adhesive material demonstrates sufficient bonding force, and during 150 of less thaies, can suppress to follow bonding operation that the caused generation gas of chemical transformation takes place owing to carbonate group or acid halide group, thereby can improve bonding force, suppress the inhomogeneous of bonding force.In addition, by making 150 of number less thaies that contain the carbonyl functional group, can improve the thermotolerance and the resistance to chemical reagents of fluorine-containing adhesive material.
In addition, the number that contains the carbonyl functional group that contains in the vinyl fluoride polymkeric substance of the present invention, because the form of the kind of bonded material, shape, bonding purpose, purposes, necessary bonding force, fluorine-containing adhesive material and adhesive bonding methods etc. is different, can in the scope of 150 of less thaies, select aptly, but the number that preferably contains the carbonyl functional group is with respect to carbonatoms 1 * 10
6Individual is 100 of less thaies, and more preferably less than is 80,50 of preferred especially less thaies.Containing the following of carbonyl functional group and be limited to 10, be preferably 20, for example can be 30.
Fluorine-containing adhesive material not only demonstrates good initial stage bonding force, and for temperature variation (under low temperature or high temperature, using etc.), soaking into of water, medicine or solvent etc. also demonstrated favorable durability.
The carbonate group that contains in the vinyl fluoride polymkeric substance of the present invention, generally be have-OC (=O) group of O-key, its concrete structure for-OC (=O) the O-R group [R is hydrogen atom, organic group (C for example
1～C
20Alkyl (C particularly
1～C
10Alkyl), the C that has ehter bond
2～C
20Alkyl etc.) or I, II, VII family element].The example of carbonate group preferably can enumerate-OC (=O) OCH
3,-OC (=O) OC
3H
7,-OC (=O) OC
8H
17,-OC (=O) OCH
2CH
2OCH
2CH
3Deng.
The acid halide group that contains in the vinyl fluoride polymkeric substance of the present invention, its concrete structure for-COY[Y is a halogen], can enumerate-COF ,-COCl etc.
In addition, the content that contains the carbonyl functional group that contains in the vinyl fluoride polymkeric substance of the present invention can be measured and calculate with infrared absorption spectrum analysis.These have the fluorine-containing adhesive material that the vinyl fluoride polymkeric substance is constituted that contains that contains the carbonyl functional group, itself can keep good characteristics such as resistance to chemical reagents that fluoropolymer has, solvent resistance, weathering resistance, didirtresistance, Abherent, the excellent characteristic that fluoropolymer is had is not given the multilayer body after bonding with not reducing.Consider that from the viewpoint of resistance to chemical reagents, solvent resistance the vinyl fluoride polymkeric substance that contains of the present invention preferably is insoluble to general solvents (being non-fluorous solvent especially) such as the ester class used in the fields such as coating, tackiness agent, ketone.In addition, said among the present invention " being insoluble to solvent " is even be meant (for example 0～100 ℃ of general employed temperature condition below the fluoro-resin fusing point and below solvent boiling point, particularly 20 ℃) under, make fluoro-resin contact and place the sufficiently long time with solvent (for example 1 hour～1 day, particularly 24 hours) time, also can be visually observed a kind of like this situation that fluoro-resin does not dissolve part.
Of the present invention containing in the vinyl fluoride polymkeric substance, contain on the end or side chain that the carbonyl functional group is bonded to polymer chain.
More specifically, can be by any formation of following (1)～(3):
(1) on the end of polymer chain or side chain, only have carbonate group, with respect to backbone c atoms several 1 * 10
6150 of individual less thaies contain the vinyl fluoride polymkeric substance,
(2) on the end of polymer chain or side chain, only have acid halide group, with respect to backbone c atoms several 1 * 10
6150 of individual less thaies contain the vinyl fluoride polymkeric substance,
(3) have carbonate group and acid halide group the two, the total number of these functional groups is with respect to backbone c atoms several 1 * 10
6Individually contain the vinyl fluoride polymkeric substance for 150 of less thaies.But more preferably adopt the concrete example of (1) or (3).Carbonate group is because extremely stable to the temperature range of mold temperature at normal temperature (20 ℃), so during the concrete example of employing (1), have the advantage of particle processing ease.In addition, because carbonate group differs widely with the speed of response of acid halide group and the complexity of reaction, thus when employing has the concrete example of (3) of two kinds of reactive groups, the wide ranges of conglutination reaction condition, bonding strength also improves.
Have the vinyl fluoride polymkeric substance that contains that contains the carbonyl functional group at the end of polymer chain and be meant in the one or both ends of polymer chain to have the polymkeric substance that contains the carbonyl functional group.On the other hand, side chain has the vinyl fluoride polymkeric substance that contains that contains the carbonyl functional group and is meant ethene monomer with carbonate-containing base and/or acid halide group and contains the monomeric copolymer structure person of vinyl fluoride beyond it.Also can all have the carbonyl functional group of containing on the end of 1 polymer chain and the side chain.
Wherein, the polymer chain end has the adhesive material that contains the carbonyl functional group, because thermotolerance, mechanical characteristics, resistance to chemical reagents are significantly reduced, owing to be favourable aspect productivity, the cost, is preferred therefore perhaps.
And, among the present invention employed end at polymer chain have contain the carbonyl functional group contain the vinyl fluoride polymkeric substance, say closely, not only can be that one or both ends by 1 polymer chain have the polymkeric substance that contains the carbonyl functional group and constitute, and can be that the polymer chain one or both ends have polymkeric substance that contains the carbonyl functional group and the mixture that does not contain carbonyl functional group's polymer chain.
In a word, even contain in the vinyl fluoride polymkeric substance exist do not contain the carbonyl functional group contain the vinyl fluoride polymkeric substance, as long as with respect to total (that is, contain carbonyl functional group contain vinyl fluoride polymkeric substance and the total amount that contains the vinyl fluoride polymkeric substance that does not contain the carbonyl functional group) backbone c atoms several 1 * 10
6Individual, have 150 of less thaies, 100 of preferred less thaies, the more preferably polymkeric substance that contains the carbonyl functional group of 80 of less thaies, 50 of preferred especially less thaies, just can not destroy binding property with various materials.
The selection that kind that contains the vinyl fluoride polymkeric substance of the present invention and structure can suit according to purpose, purposes, using method etc., wherein, preferred its crystalline melt point or second-order transition temperature are below 270 ℃, particularly when adopting the bonding processing of heating and melting to carry out lamination, the binding property that contains carbonyl functional group and other material can be given play to greatest extent, thereby the direct firm bonding force with base material can be given.In addition, preferably, when crystalline melt point or glass transformation temperature below 230 ℃, more preferably below 210 ℃, for example below 200 ℃ the time, can carry out lamination with the relatively poor organic materials of thermotolerance.
Also have, said among the present invention " crystalline melt point " and " second-order transition temperature " when detected polymkeric substance is crystalline and detects crystalline melt point in DSC described later measures, are meant crystalline melt point, and when in DSC measures, not detecting crystalline melt point, be meant second-order transition temperature.
Containing the vinyl fluoride polymkeric substance is a kind of polymkeric substance (homopolymer or multipolymer) with the repeating unit that contains the vinyl fluoride monomer derived by a kind at least and come.
Contain the vinyl fluoride monomer for having the alkene unsaturated monomer of 1 fluorine atom at least, be specially tetrafluoroethylene, vinylidene, a chlorotrifluoroethylene, vinyl fluoride, R 1216, hexafluoro-isobutene, formula (ii) shown in monomer:
CH
2＝CX
1(CF
2)
nX
2????(ii)
[in the formula, X
1Be H or F, X
2Be H, F or Cl, n is 1～10 integer.] and perfluor (alkyl vinyl ether) class etc.
In addition, the vinyl fluoride polymkeric substance that contains of the present invention also can be to have the above-mentioned multipolymer that contains the ethene monomeric unit of vinyl fluoride monomeric unit and free-floride.
The monomeric amount ratio of ethene that contains vinyl fluoride monomer and free-floride can be 10～100 moles of % (for example 30～100 moles of %) and 0～90 mole of % (for example 0～70 mole of %).
For performances such as thermotolerance and resistance to chemical reagents are reduced, floride-free ethene monomer is preferably selected from the ethene monomer of carbonatoms below 5.Can enumerate ethene, propylene, 1-butylene, 2-butylene, vinylchlorid, vinylidene chloride etc. particularly.
Wherein, aspect thermotolerance, resistance to chemical reagents, preferably with tetrafluoroethylene units as neccessary composition contain the vinyl fluoride polymkeric substance, aspect forming process, preferably contain the vinyl fluoride polymkeric substance as neccessary composition with the vinylidene unit.
Of the present invention containing in the vinyl fluoride polymkeric substance, can wait crystalline melt point or the second-order transition temperature of adjusting polymkeric substance, and then can form in arborescens or the elastomerics shape material any by selecting to contain the monomeric kind of vinyl fluoride, combination, ratio of components.Can select to contain the proterties of vinyl fluoride polymkeric substance aptly according to the purpose or the purposes of adherent purpose or purposes, multilayer body.
As the preferred object lesson that contains the vinyl fluoride polymkeric substance, can enumerate:
(I) contain tetrafluoroethylene units and ethylene unit multipolymer,
(II) contain the unitary polymkeric substance of vinylidene and
(III) contain the multipolymer of monomeric unit shown in tetrafluoroethylene units and the formula (i):
CF
2＝CF-Rf
1????(i)
[in the formula, Rf
1Be CF
3Or ORf
2(Rf
2Perfluoroalkyl for carbonatoms 1～5.)]。
As the multipolymer that contains tetrafluoroethylene units and ethylene unit (I), can enumerate a kind of like this multipolymer that contains the carbonyl functional group that has, wherein, with respect to for the whole monomers having the monomer that contains the carbonyl functional group when containing the carbonyl functional group (side chain have), tetrafluoroethylene units is 20～90 moles of % (for example 20～60 moles of %), ethylene unit is 10～80 moles of % (for example 20～60 moles of %), and can be 0～70 mole of % with the monomeric unit of their copolymerization.
But as the monomer of copolymerization, can enumerate R 1216, a chlorotrifluoroethylene, formula (ii) shown in monomer:
CH
2＝CX
1(CF
2)
nX
2????(ii)
[in the formula, X
1Be H or F, X
2Be H, F or Cl, n is 1～10 integer.] perfluor (alkyl vinyl ether) class and propylene etc., use usually in them more than a kind or 2 kinds.
These are given an example have contain the carbonyl functional group contain the vinyl fluoride polymkeric substance, be particularly preferred aspect the excellent propertys such as thermotolerance, resistance to chemical reagents, weathering resistance, electrical insulating property and non-binding property.
Wherein, following multipolymer is lower at the premium properties that can keep the tetrafluoroethylene/ethylene multipolymer, fusing point, and the binding property of other materials is good etc., and the aspect is preferred:
(I-1) multipolymer that contains the carbonyl functional group by having of constituting of 62～80 moles of % of tetrafluoroethylene units, 20～38 moles of % of ethylene unit, 0～10 mole of % of other monomeric units,
(I-2) has a multipolymer that contains the carbonyl functional group by what 20～80 moles of % of tetrafluoroethylene units, 10～80 moles of % of ethylene unit, 0～30 mole of % in R 1216 unit, 0～10 mole of % of other monomeric units constituted.
As containing the unitary polymkeric substance of vinylidene (II), with respect to for the whole monomers having the monomer that contains the carbonyl functional group when containing the carbonyl functional group (side chain have), preferred example is to have a multipolymer that contains the carbonyl functional group by what 0～30 mole of % at least a unit in 10～100 moles of % in vinylidene unit, 0～80 mole of % of tetrafluoroethylene units and a R 1216 or the chlorotrifluoroethylene constituted.
More specifically, preferably can enumerate following polymkeric substance:
(II-1) has the polyvinylidene difluoride (PVDF) (PVdF) that contains the carbonyl functional group
(II-2) has a multipolymer that contains the carbonyl functional group by what 30～99 moles of % in vinylidene unit, 1～70 mole of % of tetrafluoroethylene units constituted
(II-3) has a multipolymer that contains the carbonyl functional group by what 60～90 moles of % in vinylidene unit, 0～30 mole of % of tetrafluoroethylene units, 1～20 mole of % in a chlorotrifluoroethylene unit constituted
(II-4) has a multipolymer that contains the carbonyl functional group by what 60～99 moles of % in vinylidene unit, 0～30 mole of % of tetrafluoroethylene units, 1～10 mole of % in R 1216 unit constituted
(II-5) has multipolymer that contains the carbonyl functional group etc. by what 15～60 moles of % in vinylidene unit, 35～80 moles of % of tetrafluoroethylene units, 5～30 moles of % in R 1216 unit constituted.
Contain vinylidene unitary have contain the carbonyl functional group contain vinyl fluoride polymkeric substance (II), excellent propertys such as its weathering resistance, and then owing to can carry out forming process at low temperatures are so can carry out lamination with the so not good organic materials of thermotolerance etc.
As polymkeric substance (III), be following multipolymer:
(III-1) multipolymer that contains the carbonyl functional group by having of constituting of 65～95 moles of % of tetrafluoroethylene units, preferred 75～95 moles of %, 5～35 moles of % in R 1216 unit, preferred 5～25 moles of %,
(III-2) by tetrafluoroethylene units 70～97 moles of %, CF
2=CFORf
2(Rf
2Perfluoroalkyl for carbonatoms 1～5) 3～30 moles of % in unit constitute have the multipolymer that contains the carbonyl functional group,
(III-3) be by tetrafluoroethylene units, R 1216 unit, CF
2=CFORf
2(Rf
2Identical with above-mentioned definition) unit constitute have a multipolymer that contains the carbonyl functional group, wherein, R 1216 unit and CF
2=CFORf
2The multipolymer that unitary total amount is 5～30 moles of % etc.
These also are so-called perfluor based copolymers, and in fluoropolymer, performances such as its thermotolerance, resistance to chemical reagents, hydrophobicity, Abherent, electrical insulating property are also best.
Of the present invention contain the vinyl fluoride polymkeric substance can by will have the ethene monomer that contains carbonyl functional group's or derivatives thereof with meet fluoropolymer that purpose forms contain the vinyl fluoride monomer and/or non-vinyl fluoride monomer copolymerization obtains.Be on the other hand for obtain the polymer molecule end have contain the carbonyl functional group contain the vinyl fluoride polymkeric substance, can adopt the whole bag of tricks, wherein, aspect economy and quality aspects such as thermotolerance, resistance to chemical reagents, preferably adopting peroxycarbonates is the method that superoxide is used as polymerization starter.
As being used to import the peroxycarbonates that end contains the carbonyl functional group, preferably use the compound shown in following formula (1)～(4):
[in the formula, R and R ' " are the straight chain shape of carbonatoms 1～15 or a catenate divalent saturated hydrocarbon base or a terminal straight chain shape or a catenate divalent saturated hydrocarbon base that contains the carbonatoms 1～15 of alkoxyl group for straight chain shape or a catenate univalent saturated hydrocarbon radical or a terminal straight chain shape or a catenate univalent saturated hydrocarbon radical that contains the carbonatoms 1～15 of alkoxyl group of carbonatoms 1～15, R.]。
Preferred especially peroxy dicarbonate di-n-propyl ester, tert-butyl hydroperoxide sec.-propyl carbonic ether, two (4-tert-butylcyclohexyl) peroxy dicarbonate, two-2-ethylhexyl peroxy dicarbonate etc.
The consumption of peroxycarbonates is according to the kind of the kind of purpose polymers (form etc.), molecular weight, polymerizing condition, employed peroxycarbonates and difference, for polymkeric substance 100 weight parts that polymerization obtains, be preferably 0.05～20 weight part, be preferably 0.1～10 weight part especially.
As polymerization process, industrial preferred employing suspension polymerization, wherein, use contains fluorine series solvent, and peroxycarbonates as polymerization starter, is carried out in aqueous medium, but also can adopt other polymerization process, for example solution polymerization, letex polymerization, mass polymerization etc.
In the suspension polymerization, except water, can use to contain fluorine series solvent.As employed fluorine series solvent in the suspension polymerization, can use hydrogen chlorofluoromethane hydro carbons (CH for example
3CClF
2, CH
3CCl
2F, CF
3CF
2CCl
2H, CF
2ClCF
2CFHCl), chlorofluoromethane hydro carbons (CF for example
2ClCFClCF
2CF
3, CF
3CFClCFClCF
3), perfluoro alkane class (for example perfluorocyclobutane, CF
3CF
2CF
2CF
3, CF
3CF
2CF
2CF
2CF
3, CF
3CF
2CF
2CF
2CF
2CF
3), wherein preferred perfluoro alkane class.The consumption of fluorine series solvent, the suspension stability during from polymerization, economy aspect are considered, are preferably 10～100 weight % of water.
There is no particular limitation for polymerization temperature, can be 0～100 ℃.
Polymerization pressure can determine aptly, can be 0～100kgf/cm usually according to other polymerizing conditions such as employed solvent types, consumption and vapour pressure, polymerization temperatures
2G.
Making of the present inventionly when containing the vinyl fluoride polymkeric substance, in order to regulate molecular weight, can use common chain-transfer agent, for example hydro carbons such as iso-pentane, Skellysolve A, normal hexane, hexanaphthene; Alcohols such as methyl alcohol, ethanol; Halogenated hydrocarbons such as tetracol phenixin, chloroform, methylene dichloride, methyl chloride.
The content of terminal carbonate group can be controlled by regulating polymerizing condition.Particularly can wait and control by consumption, the consumption of chain-transfer agent, polymerization temperature as the peroxycarbonates of polymerization starter.
Contain the vinyl fluoride polymkeric substance for what obtain that the polymer molecule end has an acid halide group, can adopt the whole bag of tricks, for example, can obtain by the carbonate group that contains the vinyl fluoride polymkeric substance (decarbonate) that above-mentioned those ends of thermal degradation have a carbonate group.
Heating temperature according to the kind of carbonate group, contain the vinyl fluoride polymkeric substance kind and difference wishes polymkeric substance itself is heated to more than 270 ℃, preferred more than 280 ℃, preferred especially more than 300 ℃.The upper limit of Heating temperature preferably is in below the heat decomposition temperature at the position beyond the carbonate group that contains the vinyl fluoride polymkeric substance, is specially below 400 ℃, is preferably especially below 350 ℃.
The vinyl fluoride polymkeric substance that contains of the present invention, in order not destroy binding property, thermotolerance and the resistance to chemical reagents etc. that itself have, preferably be used for adhesive material separately, but can in the scope of not destroying its performance, cooperate various weighting agents such as inorganic powder, glass fibre, carbon fiber, metal oxide or carbon according to purpose and purposes.In addition, except weighting agent, can also hybrid pigment, UV light absorber, other additives arbitrarily.Except additive, also can cooperate other fluoro-resin or resins such as thermoplastic resin, thermosetting resin, synthetic rubber etc., can reach thus and improve mechanical characteristics, improve weathering resistance, give ornamental, antistatic, as to improve formability etc. purpose.
By containing the fluorine-containing adhesive material that the vinyl fluoride polymkeric substance constitutes, can use with the film or the various forms such as sheet material, moulding product or aqueous dispersion, organic solvent dispersion of powder or particle, moulding in advance.
By these fluorine-containing adhesive materials that are processed to different shape are contacted with other materials, and the operation that for example keeps heating and pressurizing state etc., good tacky state between fluorine-containing adhesive material and other materials, formed thus.Particularly, can obtain firm bonding force by fluorine-containing adhesive material of the present invention is contacted with other materials with the heating and melting state.
In the fluorine-containing adhesive material of the present invention, material that particularly can melt molding, itself can be used as formed material, can adopt the known in the past forming methods such as insert moulding of injection molding, extrusion moulding, inflation moulding, coating, use mould etc. to make the moulding product.In addition, also can adopt co-extrusion modling directly to make the multilayer body of shapes such as film, sheet material, tubing, flexible pipe.In addition, can also make earlier film or sheet material, again this film or sheet material be carried out lamination with other materials, thus the manufacturing multilayer body.
The of the present invention various fluorine-containing adhesive materials of more than enumerating also can be used for the surface treatment of powder or use as coating.
For example, fluorine-containing adhesive material of the present invention is made powder or aqueous dispersion, organic solvent dispersion, can make the composition that coating is used thus, utilize fluorine-containing adhesive material that have with binding propertys various materials, the silane coupling agent that can use as fluoro-containing coating.
Among the present invention, above-mentioned fluorine-containing adhesive material can be formed as fluorine-containing adhesive films (below be also referred to as " adhesive films ").
From rationalization, the automatization of the exploitation of matrix material, bonding operation, prevent that viewpoint such as public hazards from considering that hotmelt is developed, but general hotmelt must use coating machine.In contrast, the film like tackiness agent does not need coating machine, be placed on the base material or be clipped in carry out hot pressing between the base material just can be bonding, therefore operation is simple, is favourable.In addition, owing on whole of base material, form uniform bonding coat, therefore can obtain uniform bonding force and can not take place bonding irregularly, also can be used to not have bonding between the base material of intermiscibility or intermiscibility difference.And then it can also be cut into different shape and use, the loss of work is few, and operating environment is good, also is favourable on cost.
Adhesive films of the present invention has above-mentioned advantage.
In the fluorine-containing adhesive material shown in above-mentioned, can be according to purposes and purpose, thin film fabrication operation, adhesive bonding method, make adhesive films with various fluorine-containing adhesive materials, but adhesive films itself have thermotolerance, resistance to chemical reagents, mechanical characteristics, the Abherent under the multilayer body use temperature etc.; Can carry out with melt molding etc. expeditiously is the film forming of representative, in general fluoro-resin, has good formability at a lower temperature, can form thin and film uniformly; Moreover, can adopt the legal fusion at a lower temperature of various hot pressing, firmly and neatly be adhered on the various base materials, since above these reasons, the preferred use by above-mentioned multipolymer (I), (II) or the fluorine-containing adhesive material that (III) constitutes and then the preferred particularly fluorine-containing adhesive films that uses the fluorine-containing adhesive material that constitutes by above-mentioned (I-1), (I-2), (II-1), (II-2), (II-3), (II-4), (III-1), (III-2), (III-3) to carry out melt molding and obtain.
The thickness of fluorine-containing adhesive films of the present invention can be selected according to purpose and purposes, does not have special limit, but is generally 1～3000 μ m, is preferably 3～500 μ m, is preferably 5～300 μ m especially.
Crossing thin film needs special manufacture method, when carrying out bonding operation, and operational difficulty, and cause gauffer or breakage, bad order easily, and also bonding strength, physical strength, resistance to chemical reagents, weathering resistance aspect are also insufficient sometimes.Unfavorable aspect the operation of blocked up film in cost, bonding process.
Further, the layer that the present invention can be made of (A-1) above-mentioned fluorine-containing adhesive material and (D-1) by do not have contain the carbonyl functional group contain that the vinyl fluoride polymkeric substance constitutes layer carry out lamination, make fluorine-containing adhesive multilayer film (below be also referred to as " adhesive multilayer film ").
Promptly, surface has binding property with other base materials owing to having the fluorine-containing adhesive material that the vinyl fluoride polymkeric substance constitutes of containing that contains the carbonyl functional group, the layer of another surface for constituting by common fluoropolymer, contact with base material by the face that makes fluorine-containing adhesive material, operation makes it bonding through hot pressing etc., can give base material with good characteristics such as the good resistance to chemical reagents of fluoropolymer, solvent resistance, weathering resistance, stain resistance, Abherent, low frictional properties, electrical characteristic thus or contain the multilayer body of base material.
In the adhesive multilayer film that lamination forms of the present invention and (D-1), contain vinyl fluoride polymkeric substance (D-1) and can be selected from polytetrafluoroethylene (PTFE), tetrafluoroethylene-perfluor (alkyl vinyl ether) based copolymer (PFA), hexafluoropropylene (HFP)/tetrafluoroethylene (TFE) based copolymer (FEP), ethylene-tetrafluoroethylene based copolymer (ETFE), ethene-one chlorotrifluoroethylene based copolymer (ECTFE), polyvinylidene difluoride (PVDF) (PVdF), vinylidene based copolymer etc. particularly (A-1).With (A-1) during with (D-1) lamination, when perhaps making itself and other materials bonding, in order to keep and utilize the good formability and the bonding processibility of adhesive multilayer film of the present invention, (D-1) be preferably selected from crystalline melt point or second-order transition temperature and containing the vinyl fluoride polymkeric substance below 270 ℃.Can give base material with the good characteristic of above-mentioned fluoropolymer thus or contain the laminate of base material, be preferred.
Of the present invention the material that constitutes each layer can carry out various selections according to purpose, purposes, working method etc. by in 2 layers of adhesive multilayer film that constitutes, the good combination of preferred binding property, intermiscibility.
Specifically, having fusible layer (A-1) in 2 layers is preferably selected to be similar at composition and introduces those polymkeric substance of giving the fusible carbonyl functional group of containing containing of layer (D-1) in the vinyl fluoride polymkeric substance.
More particularly,
I) not only have good thermotolerance, resistance to chemical reagents, solvent resistance, mechanical properties but also melt molding excellent processability aspect, the preferred fluorine-containing adhesive multilayer film that forms by the formed layer laminate of multipolymer that with tetrafluoroethylene units, ethylene unit is main component of the formed layer of fluorine-containing adhesive material that constitutes by above-mentioned multipolymer (I) by (A-1) and (D-1).
Ii) weathering resistance, solvent resistance, forming process good aspect, the preferred fluorine-containing adhesive multilayer film that forms by the formed layer laminate of at least a kind of polymkeric substance that is selected from PVdF, the vinylidene based copolymer of the formed layer of fluorine-containing adhesive material that constitutes by above-mentioned polymkeric substance (II) by (A-1) and (D-1).
Iii) Abherent when thermotolerance, solvent resistance, resistance to chemical reagents, multilayer body are used and hydrophobicity good especially aspect, preferably the formed layer of fluorine-containing adhesive material that constitutes by above-mentioned polymkeric substance (III) by (A-1) with (D-1) by 75～100 moles of % of tetrafluoroethylene units and formula (i):
CF
2＝CFRf
1?????(i)
[in the formula, Rf
1Be CF
3Or ORf
2(Rf
2Perfluoroalkyl for carbonatoms 1～5.)]。Shown in the fluorine-containing adhesive multilayer film that forms of the formed layer laminate of polymkeric substance that constitutes of 0～25 mole of % of monomeric unit.
Thickness by 2 layers of adhesive multilayer film that constitutes of the present invention can be selected according to purpose and purposes, and there is no particular limitation, but 2 lamination meter thickness are 5～5000 μ m, are preferably 10～1000 μ m, are preferably 12～500 μ m especially.
The thickness of each layer can be binder layer (A-1) 1～1000 μ m, contain about vinyl fluoride polymer layer (D-1) 4-4995 μ m, be preferably binder layer (A-1) 3～500 μ m, fluoropolymer layer (D-1) 5～990 μ m, more preferably (A-1) 5～200 μ m, (D-1) 10～490 μ m.
Among the present invention, also can in the scope of destruction characteristic not, make at least 1 layer in adhesive films and the adhesive multilayer film to contain suitable toughener, weighting agent, stablizer, UV light absorber, pigment and other suitable additive.By adding these additives, also can improve thermostability, surface hardness, wear resistant, weathering resistance, charging property, and improve other characteristic.
Adhesive films of the present invention can be according to the wherein kind of employed polymkeric substance and the shape of purpose film, adopts the various manufacture method such as method that obtain continuous film after pressure sintering, extrusion molding, cutting system or application powder, water-based or the organic solvent dispersion etc. to obtain.
For example, even of the present invention to have the fluorine-containing adhesive material that contains the carbonyl functional group be the sort of adhesive material that also has good melt molding under lower temperature, therefore, can adopt methods such as compressed moulding, extrusion moulding, consider that from reasons such as productivity and quality aspects melt extruding moulding is particularly preferred method.
Engaging of adhesive multilayer film by 2 layers of formation of (A-1) and (D-1) of the present invention is integrated, can adopt (A-1) overlaped with (D-1) form film separately and carry out the method for compressed moulding or on side's form film coating the opposing party method, utilize the co-extrusion modling method in film forming, to finish the incorporate method etc. that engages, wherein, aspect productivity and quality, the preferred multi-layer co-extruded method of forming.
Adhesive films of the present invention and adhesive multilayer film and other material bonding is to adopt heating to wait to carry out thermal activation to finish, and more preferably heat fusing is bonding.Especially, fluorine-containing adhesive material of the present invention can demonstrate particularly the firm bonding force with other material when heat fusing is bonding.As representational adhesive bonding method, hot-rolling method, pressure sintering, ratio-frequency heating method, vacuum pressing-combining method (vacuum pressing etc.), air platen press etc. are arranged, when other material is thermoplastic resin, representational is coetrusion for example, can select aptly according to the shape of the kind of other material and shape, film and kind etc.
Adhesive films of the present invention and adhesive multilayer film are made of aforesaid different shape, size, thickness etc., and the good characteristic owing to good binding property and fluoropolymer to various materials are had can be used in the purposes of wide region.Can be used as the protection coating material of for example metallic substance; specifically; be applicable to the protection against corrosion adhesive tape that is wrapped on the chemical devices pipe arrangement, the protection against corrosion adhesive tape that is wrapped in the chemical devices tank base, the etch-proof adhesive tape of pipe arrangement, other pipe arrangement that is used for boat deck etc. requires the purposes and the good inner decoration material of stain resistance of weathering resistance with the roof in greenhouse or sidewall, decorative material, solar cell surface etc. with protection against corrosion adhesive tape, billboard, agricultural.Further, also can be used for the purposes that food product pack, drug packaging etc. require resistance to chemical reagents.
In addition, purposes that purposes that the stationary roll of duplicating machine, printer etc. and backer roll, food processing apparatus, cooking machine etc. require Abherent and low frictional properties, tellite etc. require electrical characteristic, Hydrophobic glass etc. be can also be used for and liquid crystal associated materials such as hydrophobic purposes and liquid-crystal display and automobile associated materials etc. required.
Further, the invention still further relates to a kind of multilayer body that formed layer of above-mentioned fluorine-containing adhesive material and the formed layer laminate of other material are formed.
Of the present invention have the fluorine-containing adhesive material (A) that contains the carbonyl functional group, even multiple material such as various inorganic materials or organic materials does not carry out above-mentioned surface treatment etc., also can be directly and they are bonding well, thus form various multilayer body.
The 1st multilayer body of the present invention (below be also referred to as " multilayer body 1 ") by (A-2) by the formed layer of above-mentioned fluorine-containing adhesive material and (B-1) by layer (A-2) with particularly have and contain formed layer of multilayer body of forming of organic materials that the carbonyl functional group demonstrates affinity or reactive functional group.
The thickness of multilayer body 1 can be 10～10000 μ m, is preferably 15～4000 μ m.The thickness of the layer of fluorine-containing adhesive material (A-2) can be 1～2000 μ m, is preferably 3～1000 μ m.The thickness of organic material layer (B-1) can be 5～9000 μ m, is preferably 10～3000 μ m.
Promptly, fluorine-containing adhesive material of the present invention (A-2), because the effect that contains the carbonyl functional group that is contained, also can give good binding property for the organic materials beyond the fluoropolymer, wherein, those contain with (A-2) in contain the organic materials that the carbonyl functional group has the functional group of reactivity or affinity, aspect the bonding force of (A-2), be preferred.
Organic materials in the multilayer body 1 of the present invention is natural organic matter or their mixtures such as synthesized polymer materials such as synthetic resins, synthetic rubber, synthon, synthetic leather, natural rubber, natural fiber, timber, stationery, leather-like.
Wherein, non-fluorine based polymer material becomes the performance of defective separately by replenishing mutually with the fluoropolymer lamination, thereby can be used in the various uses, is preferred in this.
Non-fluorine based polymer can be enumerated for example polyester, polymeric amide, polyphenylene sulfide, acrylic acid polymer, the vinyl acetate between to for plastic based polymer, polyolefine, vinyl chloride-based polymer, polycarbonate, styrenic, urethane, acrylonitrile butadient styrene (ABS), polyimide, polyamidoimide, polyether-ether-ketone (PEEK), polyethersulfone (PES), polysulfones, polyphenylene oxide (PPO), polyaramide, polyacetal, polyetherimide, silicone resin, Resins, epoxy, resol, aminoresin, unsaturated polyester, derivatived cellulose etc.
Wherein, 1. containing in the molecule and contain the polymer materials that the carbonyl functional group has the functional group of reactivity or affinity, is being preferred aspect the binding property of fluorine-containing adhesive material of the present invention.Among the present invention, and contain the carbonyl functional group and have reactive functional group, be meant when adopting the aftermentioned condition of molding, when moulding, can react and form the functional group of chemical bond with carbonate group and/or acid halide group.In addition, be meant and demonstrate the to a certain degree functional group of intermolecular forces with carbonate group and/or acid halide group isopolarity group with containing the functional group that the carbonyl functional group has affinity, and be functional group with at least 1 atom except that carbon atom and hydrogen atom.Specifically, preferably has hydroxyl, carboxyl, metal carboxylate, ester group, carbonate group, amino, amide group, imide, sulfydryl, thiolic acid ester group (functional group such as チ オ レ-ト), sulfonic group, Sulfonates, epoxy group(ing).2. the polymer materials of excellent heat resistance at the necessary high mold temperature of tolerance fluoro-resin, keep the thermotolerance of multilayer body integral body, can obtain to have concurrently the fluoropolymer good characteristic and is preferred as the multilayer body aspect of compatibility material polymers feature.3. thermoplastic resin can carry out simultaneously aspect the bonding and moulding of fluorine-containing adhesive material of the present invention, promptly, but be preferred aspect the multilayered molten moulding, wherein, crystalline melt point is below 270 ℃, further at the thermoplastic resin below 230 ℃, because applicable to multi-layer formings such as coextrusion, and the multilayer body that obtains demonstrates good binding property, is preferred therefore.
Specifically, ethene polymerss such as preferred polyamide, polyester, polycarbonate, polyamidoimide, PES, polysulfones, PPO, polyetherimide, polyacetal, polyvinyl alcohol, ethylene-vinyl alcohol copolymer, epoxy modifying polyethylene etc., wherein, mechanical characteristics good at melt molding, polymkeric substance itself is good, and then can be preferably polymeric amide, polyester, polycarbonate etc. by giving good resistance to chemical reagents, solvent resistance, solvent pressuretightness, weathering resistance, didirtresistance, optical characteristics aspects such as (low-refractions) with the fluoro-resin laminationization.
Wherein, preferred polyamide as the concrete example of polymeric amide, can be enumerated (1) polyamide-based resin, (2) polyamide-based elastomerics, (3) polyamide-based resin alloy etc.
Concrete example is as follows.
(1) adopts the polyamide-based resin of following method synthetic: the ring-opening polymerization of annular aliphatic lactan; The condensation polymerization of aliphatics and/or alicyclic diamine and aliphatics and/or alicyclic di-carboxylic acid; The condensation polymerization of aminocarboxylic acid; The di-carboxylic acid of the carbonatoms 36 that obtains with the unsaturated fatty acids dimerization is the so-called dimeracid of main component and short chain diprotic acid and with the copolymerization of two amines etc.
The polymkeric substance of for example nylon 6, nylon 66, Ni Long11, nylon 12, NYLON610, nylon 612, nylon 6/66, nylon 66/12, nylon 46 and m-xylene diamine/hexanodioic acid be can enumerate or monomer class and the multipolymer of dimeracid and their blend etc. of these polymeric amide constituted.
The molecular-weight average of polyamide resin is generally 5,000～500, and 000.In these polyamide resins, what be preferred for stacked tube of the present invention is polymeric amide 11,12,610,612.
(2) ABA block type polyether ester amides, polyetheramides and the polyesteramide that the polymeric amide composition is formed as soft segment as the crystallinity rigid chain segment, with polyethers or polyester as elastomeric polyamide elastomer.These elastomericss for example can adopt laurolactam and di-carboxylic acid and poly-1, and the 4-butyleneglycol carries out condensation reaction and obtains.
The carbonatoms of rigid chain segment part polymeric amide repeating unit, the chemical structure of soft segment part repeating unit and the ratio of rigid chain segment and soft segment or the molecular weight of each block can freely design according to flexibility and elastic recovery.
(3) polyamide-based alloy
(3.1) polyamide/polyolefine is an alloy
For example, Na イ ロ Application EX1020 of the ノ パ ミ Star De ST220 of the レ オ Na 4300 of the ザ イ テ Le ST of DuPont corporate system, Asahi Kasei Corporation's system, Mitsubishi chemical Co., Ltd's system, the ユ ニ チ カ of Co., Ltd. system etc.
(3.2) polymeric amide/polypropylene-based alloy
For example, the シ ス テ マ-S of clear and electrician's system.
(3.3) polymeric amide/ABS is an alloy
For example, the ト ヨ ラ ッ Network SX of eastern レ Co., Ltd. system.
(3.4) polymeric amide/polyphenylene oxide is alloy
For example, レ マ ロ イ B40 of the plastic ノ リ of Japanese GE Le GTX600, Mitsubishi chemical Co., Ltd's system etc.
(3.5) polymeric amide/polyacrylic ester is an alloy
For example, the X9 of the ユ of Co., Ltd. ニ チ カ system.
In addition, by the multilayer body 1 that fluorine-containing adhesive material of the present invention (A-2) and organic materials (B-1) constitute, the layer (D) that can further on that side lamination of fluorine-containing adhesive material (A-2), constitute by the fluoropolymer that does not contain the carbonyl functional group.
Under this occasion,, aspect mutual binding property, preferably form identical and have the vinyl fluoride polymkeric substance that contains that contains the carbonyl functional group and constitute with fluoropolymer by those as the employed fluorine-containing adhesive material of the bonding coat of this 3 layer laminate bodies.The thickness of 3 layer laminate bodies can be 25～10000 μ m, is preferably 40～4000 μ m.By fluorine-containing adhesive material constitute the layer (A-2) thickness can be 5～2000 μ m, be preferably 10～1000 μ m.By the fluoropolymer that does not contain the carbonyl functional group constitute the layer (D) thickness can be 10～5000 μ m, be preferably 15～3000 μ m.By organic materials constitute the layer (B-1) thickness can be 10～5000 μ m, be preferably 15～3000 μ m.
Promptly, this multilayer body by (A-3) by above-mentioned fluorine-containing adhesive material constituted layer, (D-2) by the layer that fluoropolymer constituted that does not contain the carbonyl functional group, with the multilayer body of (B-2) forming by the layer that above-mentioned organic materials constituted, wherein, layer (A-3) is positioned between layer (D-2) and the layer (B-2), and the formation bonding coat, this multilayer body can more effectively be given the good characteristic of fluoropolymer to organic materials.
In the multilayer body by fluorine-containing adhesive material of the present invention (A-3), fluoropolymer (D-2) and organic materials (B-2) formation, can in the scope of the characteristic of not destroying binding property, fluoropolymer and organic materials, in each layer, add suitable toughener, weighting agent, stablizer, UV light absorber, pigment and other suitable additive.These additives also can improve thermostability, surface hardness, wear resistant, weathering resistance, charging property and improve other characteristic.
Therefore, premium propertiess such as the high strength of polymeric amide, high tenacity, processibility are widely used in flexible pipe, pipe, pipeline etc.On the other hand, generally speaking, its oil-proofness is also good, but anti-alcoholic solvent poor performance, oil-proofness (ethanol petrol resistant solution) when particularly using the gasoline contain lower alcohol is poor, thereby causes swelling, and causes the material degradation of intensity reduction etc. according to different occasions.
Therefore, the past is seeking polymeric amide and fluoropolymer lamination always, thereby improves ethanol petrol resistant solution, so that as the fuel distribution tube pipe, and has carried out various researchs.For example, in order to adopt coetrusion to wait to obtain the stacked tube of polymeric amide and ETFE, composition with polymeric amide and ETFE formation is used as bonding coat (WO 95/11940 brochure, WO96/29200 brochure) often, but these adhesion-layer materials are deficiencies such as the composition that is made of polymeric amide and ETFE, the thermotolerance of itself, resistance to chemical reagents, solvent resistance.In addition, the bonding of polymeric amide and bonding coat is not to carry out bonding with chemical reaction etc., and only cause owing to being anchored effect, be subjected to the effect of adhesive layer compositions form easily, exist the bonding force problem that great changes will take place along with the environmental change of extrusion moulding condition, use temperature etc.
Fluorine-containing adhesive material of the present invention also can be bonding especially securely with polymeric amide, and the multilayer body of improving the problems referred to above can be provided.
Therefore, the multilayer body of being made up of the formed layer of formed layer of polymeric amide and the fluorine-containing adhesive material of the present invention is shaped to piped multilayered tube or flexible pipe, can be effectively as fuel distribution tube use manage, soup is with pipe or flexible pipe.
As the preferred concrete example of multilayered tube that contains aramid layer or flexible pipe, can enumerate:
I) a kind of multilayered tube or flexible pipe, it is shaped to piped multilayered tube or flexible pipe by formed layer of multilayer body of forming of the formed layer of fluorine-containing adhesive material and (B-3) polymeric amide that (A-4) above-mentioned polymkeric substance (I) constitutes, it is characterized in that layer (A-4) forms internal layer;
Ii) a kind of multilayered tube or flexible pipe, the formed layer of fluorine-containing adhesive material that it is made of (A-4) above-mentioned multipolymer (I), the formed layer of (D-3) ethylene/tetrafluoroethylene based copolymer (ETFE), the multilayer body of forming with (B-3) the formed layer of polymeric amide are shaped to piped multilayered tube or flexible pipe, it is characterized in that layer (D-3) forms innermost layer;
Iii) a kind of multilayered tube or flexible pipe, the formed layer of fluorine-containing adhesive material that it is made of (A-4) above-mentioned multipolymer (II), the multilayer body of forming with (B-3) the formed layer of polymeric amide are shaped to piped multilayered tube or flexible pipe, it is characterized in that layer (A-4) forms internal layer;
Iv) a kind of multilayered tube or flexible pipe, the formed layer of fluorine-containing adhesive material that it is made of (A-4) above-mentioned multipolymer (II), (D-3) PVdF or the formed layer of VdF based copolymer, the multilayer body of forming with (B-3) the formed layer of polymeric amide are shaped to piped multilayered tube or flexible pipe, it is characterized in that layer (D-3) forms innermost layer;
V) a kind of multilayered tube or flexible pipe, the multilayer body that it is formed by the formed layer of (B-3) polymeric amide, (A-4) above-mentioned multipolymer (I) or the formed layer of fluorine-containing adhesive material that (II) constitutes, with (B-3) the formed layer of polymeric amide is shaped to piped multilayered tube or flexible pipe, it is characterized in that layer (A-4) is positioned at the middle layer of 2 layers (B-3).
Can in the characteristic range that does not destroy purpose of the present invention, in each layer of these multilayered tube or flexible pipe, add above-mentioned weighting agent, toughener, additive etc.During especially for fuel distribution tube material and drug liquid tube, preferably the weighting agent of electroconductibility is given in interpolation in the formed layer of the fluoropolymer of internal layer ((A-4) or (D-3)).
Further, as the preferred concrete example of multilayered tube that contains aramid layer or flexible pipe, can enumerate:
Vi) a kind of multilayered tube or flexible pipe, the multilayer body that the formed layer of fluorine-containing adhesive material that it is made of (A-4) above-mentioned multipolymer (I), the formed layer of (D-3) ethylene/tetrafluoroethylene based copolymer (ETFE), (E-3) added the formed layer of ethylene/tetrafluoroethylene based copolymer (ETFE) of the weighting agent of giving electroconductibility, form with (B-3) the formed layer of polymeric amide is shaped to piped multilayered tube or flexible pipe, it is characterized in that layer (E-3) forms innermost layer.
Vii) a kind of multilayered tube or flexible pipe, the formed layer of fluorine-containing adhesive material that it is made of (A-4) above-mentioned multipolymer (I), be shaped to piped multilayered tube or flexible pipe with (D-3) the formed layer of PVdF or VdF based copolymer, the multilayer body formed with the PVdF that (E-3) has added the weighting agent of giving electroconductibility or the formed layer of VdF based copolymer, with (B-3) the formed layer of polymeric amide, it is characterized in that layer (E-3) forms innermost layer.
Concrete example is vi) and vii), and the position of each layer is from the series arrangement of innermost layer by (E-3)/(D-3)/(A-4)/(B-3).
These concrete examples are vi) and vii), tolerance effect to fuel and all kinds of SOLVENTS can freely be regulated by increasing (D-3) layer thickness, therefore, can be with as (E-3) of conductive layer layer attenuate as much as possible, thus can be with owing to add the influence that the particularly low temperature shock-resistance of (E-3) layer that the weighting agent of giving electroconductibility cause reduces and be suppressed in the inferior limit.That is, with concrete example ii) with iv) in (D-3) layer, add and give the weighting agent of electroconductibility so that innermost layer becomes the situation of conductive layer compares, concrete example vi) and vii) has the better feature of low temperature shock-resistance.
Multilayered tube of the present invention and flexible pipe can adopt various post-treatment to form required shape.For example can increase necessary parts such as joint, or adopt bending machining to form shapes such as L shaped, U-shaped, or form the shape of corrugated tube.
Further, the outside of multilayered tube of the present invention and flexible pipe also can be provided with the protective layer (F) with protection multilayered tube or flexible pipe effect.When this layer (F) is made of the material of melt-processable, can carry out simultaneously carrying out moulding and lamination in co-extrusion modling or other operation beyond the molding procedure of multilayered tube or flexible pipe with multilayered tube or flexible pipe.Constitute the material of this layer (F), as long as have the function of protection multilayered tube or flexible pipe, for example have insulativity or impact absorbency, just there is no particular limitation.
Further, as the preferred concrete example of the multilayer body of using the fluorine-containing adhesive material of the present invention, the multilayer body of forming by the formed layer of (A-5) above-mentioned fluorine-containing adhesive material (A), with (B-4) the formed layer of ethene polymers.Among the present invention, " ethene polymers " is meant the thermoplastic polymer that contains as the main composition monomer ethylene, and ethylene unit accounts for 20 moles of total monomer of polymkeric substance more than the %, is preferably 30 moles especially more than the %, for example 50 moles more than the %.Ethene polymers (B-4) more preferably contains the functional group that those and above-mentioned carbonate group or acid halide group have reactivity or affinity, particularly, preferably can enumerate epoxy modifying polyethylene, ethylene/vinyl acetate multipolymer, ethylene/vinyl alcohol copolymer, ethene/copolymer-maleic anhydride, ethylene/propene acid derivative multipolymer etc.These multilayer body and above-mentioned same can be shaped to different shape, wherein, when forming the fuel tank shape, can be used as and have for example reached resinification fuel tank for automobile in recent years, not only can improve fuel permeability, and can give thermotolerance.
Particularly, preferably can enumerate:
I) will by (A-5) by above-mentioned polymkeric substance (I) or the multilayer body formed of the fluorine-containing adhesive material that (III) constitutes and (B-4) ethene polymers be shaped to the fuel tank shape, wherein, (A-5) be positioned at the internal layer side.
Ii) will by (B4) ethene polymers, (A-5) by above-mentioned polymkeric substance (I) (II) or the fluorine-containing adhesive material that (III) constitutes and (B-4) multilayer body formed of ethene polymers be shaped to the fuel tank shape, wherein, (A-5) be positioned between 2 layers (B-4) layer.
Further, in the time of will being shaped to ampuliform by the multilayer body that fluorine-containing adhesive material of the present invention and ethene polymers are formed, utilize for example good resistance to chemical reagents of fluoropolymer, the soup bottle that uses in the time of can being used as storage and carrying various liquefied compounds (soup).Particularly employed soup in the semiconductor fabrication process owing to must suppress the composition of stripping from container so that keep high purity, is useful especially in this purposes therefore.
Particularly, preferred:
I) will by (A-5) by above-mentioned polymkeric substance (I) or the multilayer body formed of the fluorine-containing adhesive material that (III) constitutes and (B-4) ethene polymers be shaped to ampuliform, wherein, (A-5) be positioned at the internal layer side, especially preferably the layer that is made of above-mentioned polymkeric substance (III) is positioned at internal layer.
The manufacture method of multilayer body 1 of the present invention can be selected aptly according to the kind and the shape of the kind of fluorine-containing adhesive material and form, organic materials.
The method that can adopt has, and for example, makes fluorine-containing adhesive films with fluorine-containing adhesive material, and with the moulding product of organic materials overlapping after, make its thermal activation carry out the method for lamination by aforesaid heating; Perhaps, fluorine-containing adhesive material is made water-based or Liniment forms such as organic solvent dispersion, powder, and it is applied on the moulding product that organic materials makes, utilize heating to wait the method that makes its thermal activation; And insert moulding method; Perhaps when the thermoplastic polymer with fluorine-containing adhesive material of the present invention and melting moulding carries out lamination, can also adopt coetrusion etc.
Can adopt these methods multilayer body of the present invention to be shaped to shapes such as flexible pipe, pipeline, pipe, sheet material, sealing material, packing ring, wrapping material, film, fuel tank, roller, bottle, container.
Further, the invention still further relates to a kind of manufacture method of multi-layer molded articles, it is characterized in that, will have the fluorine-containing adhesive material (A) that contains the carbonyl functional group and organic materials (B) mold temperature, resin temperature when being moulding surpass respectively separately crystalline melt point or the temperature of second-order transition temperature under extrude and moulding simultaneously.That is, adopt extrusion by melting simultaneously, can (A) with moulding while of (B) bonding and purpose shape and finish continuously, so make highly productive, and bond properties is good, is preferred in this respect.
And, in the manufacture method of the present invention, the interlayer bonding force good aspect, preferred fluorine-containing adhesive material (A) and organic materials (B) all selective freezing fusing point or second-order transition temperature below 270 ℃, further at the thermoplastic resin below 230 ℃.
Further, at (A) and the outward appearance of the interlayer bonding force (B), moulding product good aspect, preferably mold temperature, resin temperature when being moulding are controlled at below 350 ℃, further are controlled at below 300 ℃.
When moulding temperature (resin temperature) is to have the crystalline melt point of the fluorine-containing adhesive material (A) that contains the carbonyl functional group or organic materials (B) or second-order transition temperature when following, any flowability of fluorine-containing adhesive material (A) or organic materials (B) all becomes insufficient, often can not reach (A) and (B) between fully bonding, and produce bad order such as formed body surface irregularity.
In addition, if mold temperature is too high, then (A) and (B) between take place bonding badly and peel off, on the formed body surface with (A) foaming and surface irregularity take place, and bad orders such as painted take place, be not preferred therefore with (B) interface.
Further, present inventors find, with crystalline melt point the fluorine-containing adhesive material (A) below 230 ℃ and thermoplastic resin (B) surpass separately crystalline melt point and under the mold temperature below 300 ℃, adopt simultaneously that extrusion by melting carries out moulding, thus can high productivity ground make (A) and (B) between have firm interlayer bonding force and have excellent appearance and the moulding product of quality.
The 2nd multilayer body of the present invention (below be also referred to as " multilayer body 2 ") by (A-5) by the formed layer of above-mentioned fluorine-containing adhesive material (A) and (C-1) by formed layer of multilayer body of forming of inorganic materials.
The thickness of multilayer body 2 can be 15～10000 μ m, is preferably 25～4000 μ m.The thickness of the formed layer of fluorine-containing adhesive material (A-5) can be 1～2000 μ m, is preferably 3～1000 μ m.The thickness of the formed layer of inorganic materials (C-1) can be 0.1～9000 μ m, is preferably 1～3000 μ m.
As inorganic materials (C-1), can enumerate metal species material and non-metal kind inorganic materials etc. particularly.
The metal species material also comprises metallic salts such as metal and the alloy type that is made of metal more than 2 kinds, metal oxide, metal hydroxides, carbonate, vitriol.Wherein, aspect binding property, more preferably metal and metal oxide, alloy type.
The kind of employed metal species material (C-1) in the multilayer body of the present invention, can enumerate metals such as aluminium, iron, nickel, titanium, molybdenum, magnesium, manganese, copper, silver, lead, tin, chromium, beryllium, tungsten, cobalt and metallic compound and, can select according to purpose and purposes by alloy type that constitutes more than 2 kinds in these etc.
As the concrete example of alloy type, can enumerate nickelalloys such as copper alloys such as aluminium alloys such as steel alloy, Al-Cl, Al-Mg, Al-Si, Al-Cu-Ni-Mg, Al-Si-Cu-Ni-Mg, brass, bronze, silicon bronze, silicon brass, German silver, nickelbronze such as carbon steel, Ni steel, Cr steel, Ni-Cr steel, Cr-Mo steel, stainless steel, silicon steel, permalloy, nickel manganese (D nickel), nickel-aluminium (Z nickel), nickel-silicon, Monel metal, constantan, inconel, haas troy alloy etc.
In addition, in order to prevent metallic corrosion etc., enterprising electroplating, hot dip process, chromizing, siliconizing, aluminising processing, sherardizing, thermospraying etc. in the metallic surface and other metal that is covered, or adopt phosphatizing to make it form the phosphoric acid salt overlay film, or make it form metal oxide, or carry out electrochemical anti-corrosive and handle by anodic oxidation or heated oxide.
And then, in order further to improve binding property, also can implement the chemical treatment of using phosphoric acid salt, sulfuric acid, chromic acid, oxalic acid etc. to the metallic surface, or implement that sandblasting, shot peening, grit blast are handled, bore and grinded, surface roughenings processing such as paper scratch (paperscratch), steel wire scratch (wirescratch) and hair processing, ornamental in order to give, can carry out painted, printing, etching etc. to the metallic surface.
In addition, good and can give good materials with function by the lamination fluoropolymer as binding property, preferred aluminum-based metal material, Ferrious material material and copper are metallic substance.
As nonmetal be inorganic materials, can enumerate sintered glass ceramics, foamed glass, heat ray-reflecting glass, the invisible heat heat absorbing glass, glass based materials such as multiple glazing, watt, large-scale porcelain plate, ceramic panel, ceramic industry class materials such as brick, granite, natural rocks such as marble, strong concrete, glass fiber-reinforced concrete (GRC), carbon fiber-reinforced concrete (CFRC), light weight bubble foamed concrete (ALC), concrete based materials such as compound ALC, extrusion moulding cement, cement based materials such as composite molding cement, other asbestos slate, hollow steel plate, silicon single crystal, polysilicon, amorphous silica, the clay class, the boron based material, carbonaceous material etc.Wherein, in binding property good and can by the lamination fluoropolymer give good function aspect, the preferred glass based material.
In the multilayer body of being made up of fluorine-containing adhesive material of the present invention (A-5) and inorganic materials (C-1) 2, preferred concrete example is as follows.
I) by (A-5) by above-mentioned multipolymer (I), (II) or the formed layer of fluorine-containing adhesive material that (III) constitutes and (C-1) by formed layer of multilayer body of forming of aluminum-based metal material.
Under this occasion, as the aluminum-based metal material, oxide compound, Al-Cu system, Al-Si system, Al-Mg system and Al-Cu-Ni-Mg system, the Al-Si-Cu-Ni-Mg that can use fine aluminium, aluminium be alloy, aldural, anticorrosion aluminium etc. casting with or the extension aluminium alloy.In addition, can also use, surface hardening anticorrosion and binding property etc. in order to improve and with the surface of caustic soda, oxalic acid, sulfuric acid, the above-mentioned aluminum or aluminum alloy of chromic acid anodizing so that its form the aluminum-based metal material (passivation aluminium) of oxide film and carry out other above-mentioned surface-treated aluminum-based metal material.
Ii) by (A-5) by above-mentioned multipolymer (I), (II) or the formed layer of fluorine-containing adhesive material that (III) constitutes and (C-1) by formed layer of multilayer body of forming of Ferrious material material.
Under this occasion,, can use pure iron, ferric oxide, carbon steel, Ni steel, Cr steel, Ni-Cr steel, Cr-Mo steel, Ni-Cr-Mo steel, stainless steel, silicon steel, permalloy, nonmagnetic steel, magnetic steel, cast iron class etc. as the Ferrious material material.
With above-mentioned same, can use the material of other metal of electroplating surface, for example hot-dip galvanized steel sheet, alloyed hot-dip galvanized steel plate, Aludip, zinc-plated nickel steel plate, zinc-plated aluminum steel plate etc.; Adopt the be covered material of other metal of impregnating method, thermal spraying method; Carrying out chromic acid system or phosphoric acid is that chemical treatment or heat treated make it form the material of oxide film; Implement the material (for example electroplating steel plate) of electric protection processing etc.
I), ii) can give erosion resistance, rust-preventing characteristic, resistance to chemical reagents, weathering resistance, Abherent and wear resistant to aluminium based material and ferrous material respectively, can be used for building materials, chemical devices with in the various uses such as machinery, cooking machinery, residential equipment associated components, tame electrical article associated components, automobile associated components, OA associated components, is preferred with material, food-processing in this respect.
Be multilayer body that metallic substance formed layer form with (C-1) by copper by the formed layer of fluorine-containing adhesive material that above-mentioned multipolymer (III) constitutes iii) by (A-5).
The water-absorbent of this multilayer body is low, can give the copper based material with the advantageous electrical properties of fluoro-resin, can be used in the purposes relevant such as tellite, electrical and electronic parts with electric and electronic, and be preferred object.
Iv) by (A-5) by above-mentioned multipolymer (I), (II) or the formed layer of fluorine-containing adhesive material that (III) constitutes and (C-1) by formed layer of multilayer body of forming of glass based material.
This multilayer body has the transparency, further gives glass surface with hydrophobicity, oleophobic property, anti-reflective, low-refraction etc., can be used for optical correlation parts, liquid-crystal display associated components, building materials glass, glass cooking machinery, vehicle glass etc.In addition, owing to have the effect that prevents glass breakage, the fire safety glass of can be used for throwing light on associated mechanical, flame retardant resistance etc. are preferred objects.
V) by (A-5) by above-mentioned multipolymer (I), (II) or the formed layer of fluorine-containing adhesive material that (III) constitutes and (C-1) by formed layer of multilayer body of forming of silicon based materials such as silicon single crystal or polysilicon or amorphous silicon.
This multilayer body has the transparency, can give weathering resistance, didirtresistance, preventing property of breakage etc. to the surface, so can be used for constituting the material of solar cell, is preferred object.
In addition, by the multilayer body 2 that fluorine-containing adhesive material of the present invention (A-5) and inorganic materials (C-1) are formed, can further not contain carbonyl functional group's fluoropolymer (D-4) at that side lamination of tackiness agent.
The thickness of 3 layer laminate bodies can be 10～10000 μ m, is preferably 15～4000 μ m.The thickness of the formed layer of fluorine-containing adhesive material (A-5) can be 1～2000 μ m, is preferably 3～1000 μ m.The thickness that does not contain carbonyl functional group's the formed layer of fluoropolymer (D-4) can be 5～5000 μ m, is preferably 10～3000 μ m.The thickness of the formed layer of inorganic materials (C-1) can be 0.1～5000 μ m, is preferably 1～3000 μ m.
Promptly, 1 multilayer body of the present invention by (A-6) by the formed layer of above-mentioned fluorine-containing adhesive material, (D-4) by the formed layer of the fluoropolymer that does not contain the carbonyl functional group and (C-2) by formed layer of multilayer body of forming of inorganic materials, and be (A-6) layer be in (D-4) layer with (C-2) layer between, form the multilayer body of bonding coat, this multilayer body can more effectively be given the good characteristic of fluoropolymer to inorganic materials.
Under this occasion, employed fluorine-containing adhesive material (A-6) in the bonding coat by 3 layers of multilayer body that constitutes 2, aspect mutual binding property, preferably constitute by the vinyl fluoride polymkeric substance that contains that those are formed with identical the having of fluoropolymer (D-4) contains the carbonyl functional group.
In the multilayer body of of the present invention and inorganic materials (C-2), also can in the scope of not destroying binding property and other characteristic of fluoropolymer, make and contain suitable toughener, weighting agent, stablizer, UV light absorber, pigment and other suitable additive in fluorine-containing adhesive material (A-6) or the fluoropolymer layer (D-4).This additive also can improve thermostability, surface hardness, wear resistant, weathering resistance, charging property, and improves other character.
The manufacture method of multilayer body 2 of the present invention can be selected aptly according to the kind and the shape of the kind of fluorine-containing adhesive material and form, inorganic materials.
The method that can adopt has, and for example, uses fluorine-containing adhesive material to make fluorine-containing adhesive films, and with inorganic materials overlapping after, make its thermal activation carry out the method for lamination by aforesaid heating; Perhaps, fluorine-containing adhesive material is made the form of water-based or Liniments such as organic solvent dispersion, powder, and it is applied on the inorganic materials, utilize heating to wait the method that makes its thermal activation; Insert moulding method etc.
Can adopt these methods that multilayer body 2 of the present invention is shaped to shapes such as flexible pipe, pipeline, pipe, sheet material, sealing material, packing ring, wrapping material, film, fuel tank, roller, bottle, container.
The preferred version of invention
Below based on reference example and embodiment the present invention is described, but the present invention is not subjected to their qualification.
In the following reference example and embodiment, be determined as follows.
(1) number of carbonate group
With the white powder of the fluoropolymer that obtains or melt extrude the particulate compressed moulding at room temperature of cutting into slices, make the thick film of 0.05～0.2mm.Adopt infrared absorption spectrum analysis to measure the 1809cm that belongs to carbonyl of the carbonate group of film (OC (=O) O-)
-1The absorbancy at peak.Calculate backbone c atoms number per 10 with following formula (1)
6The number of individual carbonate group (N).
N＝500AW/εdf??????(1)
A: from the 1809cm of carbonate group (OC (=O) O-)
-1The absorbancy at peak
ε: from the 1809cm of carbonate group (OC (=O) O-)
-1Molar absorptivity coefficient [the lcm at peak
-1Mol
-1].The ε that makes model compound is 170.
W: by monomer form calculate form the average monomer molecular weight
D: the density [g/cm of film
3]
F: the thickness of film [mm]
Also have, Perkin-Elmer FTIR spectrograph 1760X (Perkin Elmer corporate system) is used in infrared absorption spectrum analysis, scans 40 times.The IR spectrum that obtains is automatically judged baseline with Perkin-ElmerSpectrum for Windows Ver.1.4C, measures 1809cm
-1The absorbance A at peak.In addition, the thickness of film is measured with milscale.
(2) number of acyl fluorides base
Similarly the film that obtains is carried out Infrared spectroscopy with (1), measure the 1880cm that belongs to carbonyl of acyl fluorides base (C (=O) F)
-1The absorbancy at peak.Make molar absorptivity coefficient [lcm from the above-mentioned peak of acyl fluorides base
-1Mol
-1] to make ε by model compound be 600, in addition, similarly measures the number of acyl fluorides base with the formula (1) and the method for above-mentioned (1).
(3) composition of polymkeric substance
Adopt
19F-NMR measures.
(4) fusing point (Tm)
Use セ イ コ-type DSC device, the fusion peak when record heats up with the speed of 10 ℃/min, temperature that will be corresponding with peak-peak is as fusing point (Tm).
(5) MFR (melt flow rate (MFR))
Use fusion index instrument (the smart mechanism of Japan is made institute's (strain) system) is determined at specified temperature, 5kg load interior effusive polymer weight (g) of unit time (10 minutes) from the nozzle of diameter 2mm, long 8mm down.
(6) bonding stripping strength
Downcut the wide test film of 1cm from pipe, carry out 180 degree stripping tests with the speed of 25mm/min, obtain the mean value of 5 of maximums in elongation-tensile strength curve, as the bonding stripping strength of the interlayer in skin-middle layer with the Tensilon universal testing machine.
(7) outward appearance of bonding release surface
The release surface of that side of skin of the multilayered tube sample of peeling off between visual observation skin-middle layer, (being that stripper surface is smooth) of evenly peeling off are " zero ".Inhomogeneous peel off for " △ " or " * "." △ " expression stripper surface has part surface coarse.The almost whole surface irregularity of " * " expression.When stripper surface is coarse, generally can not get good bonding strength.Generation of gas etc. when this is considered to depend on moulding.
Synthesis example 1 (fluoropolymer synthetic) with carbonate group
To volume is to add pure water 200L in the enamel system autoclave of 820L, with vacuumizing after the fully displacement system of nitrogen, adds 1-fluoro-1,1-ethylene dichloride 113kg and R 1216 95kg, hexanaphthene 85g.Then, (iii) forced with nitrogen:
CH
2=CF (CF
2)
3The perfluor that H (iii) represents (1,1,5-three hydrogen-1-amylene) 292g remains on 35 ℃ with temperature in the kettle, and stirring velocity is remained on 200rpm.
Further be pressed into tetrafluoroethylene to 7.25kg/cm
2G is pressed into ethene then to 8kg/cm
2G.
Then, add 50% methanol solution 1.9kg of peroxy dicarbonate di-n-propyl ester, the beginning polymerization.Along with polymeric carries out, the still internal pressure reduces, thus append the gas mixture (mol ratio=39.2: 43.6: 17.3) that is pressed into tetrafluoroethylene/ethylene/R 1216, on one side polymerization pressure is remained 8kg/cm
2G Yi Bian proceed polymerization, in the polymerization process, divides adding formula compound 1100g (iii) 20 times with micropump, adds up to 32 hours polymerization.
After polymerization finishes, reclaim content, washing and filter after, 80 ℃ of following drying under reduced pressure 8 hours, obtain polymer powder 95kg.The rerum natura of the polymkeric substance that obtains is shown in Table 1.
Synthesis example 2 (fluoropolymer synthetic) with carbonate group
In the stainless steel autoclave of 1000L, add pure water 400L,, add perfluorocyclobutane 262kg with vacuumizing after the fully displacement system of nitrogen.Then,, temperature in the kettle is remained on 20 ℃, stirring velocity is remained on 180rpm with the forced perfluor of (iii) representing of nitrogen (1,1,5-three hydrogen-1-amylene) 2.36kg.
Further be pressed into tetrafluoroethylene to 8.57kg/cm
2G is pressed into ethene then to 9.13kg/cm
2G.Then, making temperature in the kettle is 35 ℃, and the still internal pressure is 12kg/cm
2G.
Then, add 50% methanol solution 2.3kg of peroxy dicarbonate di-n-propyl ester, the beginning polymerization.Along with polymeric carries out, the still internal pressure reduces, thus append the gas mixture (mol ratio=66: 34) that is pressed into tetrafluoroethylene/ethylene, on one side polymerization pressure is remained 12kg/cm
2G Yi Bian proceed polymerization, in the polymerization process, with the continuous supply type of micropump compound 2.4kg (iii), adds up to 15 hours polymerization.
After polymerization finishes, reclaim content, washing and filter after, 80 ℃ of following drying under reduced pressure 8 hours, obtain polymer powder 33.9kg.The rerum natura of the polymkeric substance that obtains is shown in Table 1.
Synthesis example 3 (fluoropolymer synthetic) with carbonate group and acyl fluorides base
The polymer powder that obtains in the synthesis example 1 is fed to single screw extrusion machine (limit, field plastics machinery (strain), VS50-24) (L/D=24) (screw diameter: 50mm), under near the condition of 320 ℃ of the resin temperatures 300～320 ℃ of barrel temperatures, the die head, extrude, obtain particulate material.The rerum natura of the polymkeric substance that obtains is shown in Table 1.
Synthesis example 4 (fluoropolymer synthetic) with carbonate group and acyl fluorides base
Making barrel temperature is that near 320～350 ℃, die head resin temperature is 350 ℃, in addition, similarly operates with synthesis example 2, makes particulate material with the polymer powder of acquisition in the synthesis example 1.The rerum natura of the polymkeric substance that obtains is shown in Table 1.
Synthesis example 5 fluoropolymer synthetic of carbonate group and acyl fluorides base (and have)
Carry out and synthesis example 4 identical operations, make particulate material with the polymer powder that obtains in the synthesis example 2.The rerum natura of the polymkeric substance that obtains is shown in Table 1.
Synthesis example 6 (fluoropolymer synthetic that does not contain the carbonyl functional group)
To add in the stainless steel autoclave of 500L with synthesis example 1 same synthetic polymer powder 95kg, pure water 100L, add 28% ammoniacal liquor 7kg, heat 5 hours down while stir at 80 ℃.Take out the powder of content, washing and filter after, 80 ℃ of following drying under reduced pressure 8 hours, obtain polymer powder 93kg.The rerum natura of the polymkeric substance that obtains is shown in Table 1.
Synthesis example 7 (fluoropolymer synthetic that contains carbonate group)
To internal volume is to add pure water 195.4L in the enamel system autoclave of 820L, with vacuumizing after the fully displacement system of nitrogen, adds perfluorocyclobutane 445.4kg and perfluoro methyl vinyl ether 83.0kg, tetrafluoroethylene 30.3kg.Temperature in the kettle is remained on 35 ℃, stirring velocity is remained on 150rpm.Then, be pressed into 50% methanol solution 1.0kg of peroxy dicarbonate di-n-propyl ester, the beginning polymerization with nitrogen.
Along with polymeric carries out, gaseous monomer is consumed, and still is pressed and reduced, so append the gas mixture that is pressed into tetrafluoroethylene/perfluoro methylvinylether (mol ratio=85/15), remains on 7kg/cm so that still is pressed
2(gauge pressure) carries out 34 hours polymerization.
After polymerization finishes, reclaim resultant, washing 70 ℃ of following drying under reduced pressure 10 hours, obtains polymer powder 64kg.
The powder of this polymkeric substance is fed to single screw extrusion machine (limit, field plastics machinery (strain), VS50-24) (L/D=24) (screw diameter: 50mm), under near the condition of 258 ℃ of the resin temperatures 230～240 ℃ of barrel temperatures, the die head, extrude, make particulate material.The rerum natura of the particulate material that obtains is shown in Table 1.
Synthesis example 8 (fluoropolymer synthetic that contains carbonate group)
To internal volume is to add pure water 273L in the enamel system autoclave of 820L, with vacuumizing after the fully displacement system of nitrogen, adds R 1216 164kg and tetrafluoroethylene 1.5kg.Temperature in the kettle is remained on 65 ℃, stirring velocity is remained on 200rpm.Then, be pressed into 50% methanol solution 8kg of peroxy dicarbonate di-n-propyl ester, the beginning polymerization with nitrogen.
Along with polymeric carries out, gaseous monomer is consumed, and still press to reduce, and is pressed into tetrafluoroethylene/hexafluoropropylene (gas mixture of mol ratio=86.5/13.5) is so that the still pressure remains on 4.5kg/cm so append
2(gauge pressure) carries out 60 hours polymerization.In addition, corresponding with the inactivation of peroxy dicarbonate di-n-propyl ester, be pressed into 50% methanol solution 4kg of peroxy dicarbonate di-n-propyl ester in per 30 hours.
After polymerization finishes, reclaim resultant, washing 80 ℃ of following drying under reduced pressure 8 hours, obtains polymer powder 15kg.
This polymer powder is fed to single screw extrusion machine (limit, field plastics machinery (strain), VS50-24) (L/D=24) (screw diameter: 50mm), under near the condition of 258 ℃ of the resin temperatures 230～240 ℃ of barrel temperatures, the die head, extrude, make particulate material.The rerum natura of the particulate material that obtains is shown in Table 1.
Table 1
| Monomer is formed (iii) compound/formula (i) compound of (mole %) TFE/Et/HFP/ formula | With respect to backbone c atoms several 10 6Number | Fusing point (℃) | MFR[g/10min] (mensuration temperature) | ||
| Carbonate group | The acyl fluorides base | ||||
| Synthesis example 1 | ????38.9/45.9/14.8/0.4/0 | ????411 | Do not detect | ????171.8 | ??7.1(230℃) |
| Synthesis example 2 | ????63.5/33.4/0/3.1/0 | ????556 | Do not detect | ????209.7 | ??18.4(297℃) |
| Synthesis example 3 | ????38.9/45.9/14.8/0.4/0 | ????128 | ??10 | ????171.8 | ??7.1(230℃) |
| Synthesis example 4 | ????38.9/45.9/14.8/0.4/0 | ????57 | ??30 | ????171.8 | ??7.1(230℃) |
| Synthesis example 5 | ????63.5/33.4/0/3.1/0 | ????68 | ??38 | ????209.7 | ??18.4(297℃) |
| Synthesis example 6 | ????38.9/45.9/14.8/0.4/0 | Do not detect | Do not detect | ????171.8 | ??7.1(230℃) |
| Synthesis example 7 | ????85.3/0/0/0/14.7 | ????143 | Do not detect | ????209.5 | ??12.5(265℃) |
| Synthesis example 8 | ????86.5/0/13.5/0/0 | ????135 | Do not detect | ????204.8 | ??19.5(297℃) |
TFE: the tetrafluoroethylene formula is compound (iii): CH
2=CF (CF
2)
3H
Et: ethene formula (i) compound: CF
2=CFOCF
3
HFP: R 1216
Reference example 1 (making) with fluoropolymer particles material of carbonate group
The polymer powder that obtains in the synthesis example 1 is fed to single screw extrusion machine (limit, field plastics machinery (strain), VS50-24) (L/D=24) (screw diameter: 50mm), under near the condition of 235 ℃ of the resin temperatures 190～235 ℃ of barrel temperatures, the die head, extrude, make particulate material.In the polymkeric substance that obtains, carbonate group is with respect to backbone c atoms several 1 * 10
6Individual is 381, does not detect the acyl fluorides base.
Reference example 2 (making) with fluoropolymer particles material of carbonate group
Making barrel temperature is that near 230～240 ℃, die head resin temperature is 258 ℃, in addition, carries out same operation with reference example 1, makes particulate material with the polymer powder of acquisition in the synthesis example 2.In the polymkeric substance that obtains, carbonate group is with respect to backbone c atoms several 1 * 10
6Individual is 524, does not detect the acyl fluorides base.
Reference example 3 (not containing the making of carbonyl functional group's fluoropolymer particles material)
Carry out same operation with reference example 1, make particulate material with the polymer powder that obtains in the synthesis example 6.In the particulate material that obtains, do not detect carbonate group and acyl fluorides base.
Embodiment 1 (making of multilayered tube)
Use particulate material (Ube Industries, Ltd's system of polymeric amide 12, trade(brand)name: UBE3035MI1) with synthesis example 3 in the particulate material of the fluoropolymer that obtains, outer configuration polymeric amide 12, the fluoropolymer that obtains in the intermediate adhesion layer configuration synthesis example 3, internal layer configuration electroconductibility ETFE (ダ イ キ Application industry system, trade(brand)name: EP610AS), be shaped to the multilayered tube (3 layers) of the about 8mm of external diameter, the about 6mm of internal diameter by condition shown in the table 2 with 3 kinds 3 layers while forcing machine that are equipped with the branch manifold coventry type die head coventry.The bonding stripping strength of measuring the multilayered tube that obtains with peel off after the outward appearance of adhesive interface.Test-results is shown in Table 3.
Embodiment 2
Use the particulate material of the fluoropolymer that obtains in the synthesis example 4 to replace the particulate material of the fluoropolymer that obtains in the synthesis example 3, be shaped to multilayered tube, in addition, carry out table 2 similarly to Example 1 shown in the making and the test of pipe under the condition.Test-results is shown in Table 3.
Embodiment 3
Use the particulate material of the fluoropolymer that obtains in the synthesis example 5 to replace the particulate material of the fluoropolymer that obtains in the synthesis example 3, be shaped to multilayered tube, in addition, carry out table 2 similarly to Example 1 shown in the making and the test of pipe under the condition.Test-results is shown in Table 3.
Embodiment 4
Use the particulate material of the fluoropolymer that obtains in the synthesis example 7 to replace the particulate material of the fluoropolymer that obtains in the synthesis example 3, be shaped to multilayered tube, in addition, carry out table 2 similarly to Example 1 shown in the making and the test of pipe under the condition.Test-results is shown in Table 3.
Embodiment 5
Use the particulate material of the fluoropolymer that obtains in the synthesis example 8 to replace the particulate material of the fluoropolymer that obtains in the synthesis example 3, be shaped to multilayered tube, in addition, carry out table 2 similarly to Example 1 shown in the making and the test of pipe under the condition.Test-results is shown in Table 3.
Comparative example 1
Use the particulate material of the fluoropolymer that obtains in the reference example 1 to replace the particulate material of the fluoropolymer that obtains in the synthesis example 3, be shaped to multilayered tube, in addition, carry out table 2 similarly to Example 1 shown in the making and the test of pipe under the condition.Test-results is shown in Table 3.
Comparative example 2
Use the particulate material of the fluoropolymer that obtains in the reference example 2 to replace the particulate material of the fluoropolymer that obtains in the synthesis example 3, be shaped to multilayered tube, in addition, carry out table 2 similarly to Example 1 shown in the making and the test of pipe under the condition.Test-results is shown in Table 3.
Comparative example 3
Use the particulate material of the fluoropolymer that obtains in the reference example 3 to replace the particulate material of the fluoropolymer that obtains in the synthesis example 3, be shaped to multilayered tube, in addition, carry out table 2 similarly to Example 1 shown in the making and the test of pipe under the condition.Test-results is shown in Table 3.
Table 2
| Embodiment 1 | Embodiment 2 | Embodiment 3 | Embodiment 4 | Embodiment 5 | Comparative example 1 | Comparative example 2 | Comparative example 3 | ||
| The middle layer resin | Synthesis example 3 | Synthesis example 4 | Synthesis example 5 | Synthesis example 7 | Synthesis example 8 | Reference example 1 | Reference example 2 | Reference example 3 | |
| Outermost resin | Polymeric amide 12 | ||||||||
| Inner layer resin | Electroconductibility ETFE | ||||||||
| The middle layer | Barrel temperature (℃) | 230～270 | ?230～270 | ?230～270 | ?230～270 | ?230～270 | ?230～270 | ?230～270 | ?230～270 |
| Resin temperature (℃) | 258 | ?258 | ?258 | ?258 | ?258 | ?258 | ?258 | ?258 | |
| Internal layer | Barrel temperature (℃) | 295～335 | ?295～335 | ?295～335 | ?295～335 | ?295～335 | ?295～335 | ?295～335 | ?295～335 |
| Resin temperature (℃) | 333 | ?333 | ?333 | ?333 | ?333 | ?333 | ?333 | ?333 | |
| Outer | Barrel temperature (℃) | 210～245 | ?210～245 | ?210～245 | ?210～245 | ?210～245 | ?210～245 | ?210～245 | ?210～245 |
| Resin temperature (℃) | 245 | ?245 | ?245 | ?245 | ?245 | ?245 | ?245 | ?245 | |
| Die head temperature (℃) | 280 | ?280 | ?280 | ?280 | ?280 | ?280 | ?280 | ?280 | |
| Tube draught speed (m/ branch) | 8.0 | ?8.0 | ?8.0 | ?8.0 | ?8.0 | ?8.0 | ?8.0 | ?8.0 | |
Table 3
| Embodiment 1 | Embodiment 2 | Embodiment 3 | Embodiment 4 | Embodiment 5 | Comparative example 1 | Comparative example 2 | Comparative example 3 | ||
| The middle layer resin | Synthesis example 3 | Synthesis example 4 | Synthesis example 5 | Synthesis example 7 | Synthesis example 8 | Reference example 1 | Reference example 2 | Reference example 3 | |
| Outermost resin | Polymeric amide 12 | ||||||||
| Inner layer resin | Electroconductibility ETFE | ||||||||
| Tubular shape | External diameter (mm) | ??7.98 | ??8.01 | ??8.03 | ??7.99 | ??8.03 | ????8.00 | ????8.04 | ????8.01 |
| Interior layer thickness (mm) | ??0.16 | ??0.15 | ??0.16 | ??0.17 | ??0.16 | ????0.16 | ????0.14 | ????0.15 | |
| Intermediate layer thickness (mm) | ??0.09 | ??0.10 | ??0.09 | ??0.10 | ??0.09 | ????0.09 | ????0.09 | ????0.08 | |
| Outer layer thickness (mm) | ??0.73 | ??0.69 | ??0.74 | ??0.75 | ??0.75 | ????0.74 | ????0.75 | ????0.76 | |
| Bonding strength (N/cm) | ??15.6 | ??32.7 | ??31.8 | ??30.8 | ??26.5 | ????13.0 | ????11.6 | ????0.0 *) | |
| The outward appearance of bonding release surface | ??○ | ??○ | ??○ | ??○ | ??○ | * (, having unevenness) because part is peeled off | * (, having unevenness) because part is peeled off | Not * (not bonding) | |
*) when pipe downcuts stripping test with sample, peeling off naturally
Embodiment 6
Use is equipped with 2 kinds of 2 layers of extrusion devices that the charging tubular type applies hanging type T shape die head (lip crack 800 μ m), supply with the particulate material of the fluoropolymer that obtains in the synthesis example 3 as (A) layer, supply with nylon 12 (Daicel-Huels corporate system as (B) layer, trade(brand)name: DAIAMIMIDL2101), extrude multilayer film.Then, it being attached to temperature is controlled at and makes its cooling, the thick multilayer film of continuous reeling 100 μ m on 20 ℃ the casting roller.The evaluation result of the condition of molding and the film that obtains is shown in Table 4.
And, according to following benchmark evaluation appearance of films.
Zero: can't see apparent defective fully.
△: some defective (current mark, foaming, albefaction, pinprick etc.) takes place in the area of the not enough total area 10%.
*: some defective (current mark, foaming, albefaction, pinprick etc.) takes place in the area of the total area more than 10%.
In addition, according to the binding property of following benchmark evaluation film.That is, downcut 100 of the small pieces of 5cm * 4cm from the arbitrary portion of obtaining film, try to peel off two-layer with hand with sharp cutter.
Can not peel off entirely for zero: 100.
△: 1～5 peelable.
*: peelable more than 6.
Embodiment 7
Use ethylene-vinyl alcohol copolymer (Network ラ レ system, trade(brand)name: エ バ-Le F101), in addition, extrude multilayer film similarly to Example 6, the film that obtains is estimated as (B) layer.The evaluation result of the condition of molding and the film that obtains is shown in Table 4.
Embodiment 8
Use modified polyvinyl resin (Japanese polyolefine system, trade(brand)name: レ Network ス パ-Le ET182), in addition, extrude multilayer film similarly to Example 6, the film that obtains is estimated as (B) layer.The evaluation result of the condition of molding and the film that obtains is shown in Table 4.
Comparative example 4
As the particulate material of the fluoropolymer that obtains in (A) layer use reference example 3, in addition, extrude multilayer film similarly to Example 7, the film that obtains is estimated.The evaluation result of the condition of molding and the film that obtains is shown in Table 4.
Table 4
| Embodiment | Comparative example | ||||
| ????6 | ????7 | ????8 | ????4 | ||
| Barrel temperature | The A layer | ?210～245 | ??210～245 | ??210～245 | ??210～245 |
| The B layer | ?160～245 | ??170～225 | ??150～200 | ??170～225 | |
| Die head temperature (℃) | ?235 | ??230 | ??225 | ??230 | |
| Each layer thickness (μ m) | The A layer | ?60 | ??62 | ??60 | ??60 |
| The B layer | ?40 | ??38 | ??41 | ??38 | |
| Appearance of films | ?○ | ??○ | ??○ | ??× | |
| The binding property of film | ?○ | ??○ | ??○ | ??× | |
The effect of invention
Fluorine-containing adhesive material of the present invention can bonding for example polyamide be bonding securely with base material by heating and melting. And the characteristics such as the good resistance to chemical reagents that fluoropolymer can be had, weatherability, soil resistance are given the laminated body surface, therefore, can obtain at an easy rate the good laminated body of function and various products formed.
Claims (36)
1. fluorine-containing adhesive material, it is with respect to backbone c atoms several 1 * 10 by the total number that has carbonate group and/or acid halide group, carbonate group and acid halide group on polymer chain end or side chain
6The individual vinyl fluoride polymkeric substance that contains for 150 of less thaies constitutes.
2. fluorine-containing adhesive material, it is with respect to backbone c atoms several 1 * 10 by the total number that has carbonate group and/or acid halide group, carbonate group and acid halide group on polymer chain end or side chain
6The individual vinyl fluoride polymkeric substance that contains for 100 of less thaies constitutes.
3. the fluorine-containing adhesive material described in the claim 1 or 2, wherein, on polymer chain end or side chain, with respect to backbone c atoms several 1 * 10
6Individual, have the carbonate group more than at least 10.
4. the fluorine-containing adhesive material of claim 1～3 described in each is characterized in that the number of acid halide group is with respect to backbone c atoms several 1 * 10
6Individual at least more than 10.
5. the fluorine-containing adhesive material of claim 1～4 described in each is characterized in that having carbonate group and/or acid halide group on the polymer chain end.
6. the fluorine-containing adhesive material of claim 1～5 described in each is characterized in that, contains the crystalline melt point of vinyl fluoride polymkeric substance or second-order transition temperature below 270 ℃.
7. the fluorine-containing adhesive material of claim 1～6 described in each is characterized in that, contains the crystalline melt point of vinyl fluoride polymkeric substance or second-order transition temperature below 230 ℃.
8. the fluorine-containing adhesive material of claim 1～5 described in each is characterized in that, contains the crystalline melt point of vinyl fluoride polymkeric substance or second-order transition temperature below 210 ℃.
9. the fluorine-containing adhesive material of claim 6～8 described in each is characterized in that, contains the multipolymer of vinyl fluoride polymkeric substance for being made of tetrafluoroethylene and ethene.
10. the fluorine-containing adhesive material of claim 6～8 described in each is characterized in that, contains the vinyl fluoride polymkeric substance and is the multipolymer by the formation of monomer shown in tetrafluoroethylene and the formula (i):
CF
2＝CF-Rf
1?????(i)
In the formula, Rf
1Be CF
3Or ORf
2, Rf
2Perfluoroalkyl for carbonatoms 1～5.
11. the fluorine-containing adhesive material described in the claim 9, what wherein, have carbonate group and/or an acid halide group contains the vinyl fluoride polymkeric substance for by 20～80 moles of % of tetrafluoroethylene, 10～60 moles of % of ethene and the multipolymer that can constitute with 0～60 mole of % of ethene monomer of their copolymerization.
12. the fluorine-containing adhesive material described in the claim 11, wherein, can with the ethene monomer of tetrafluoroethylene and ethylene copolymer for be selected from R 1216, a chlorotrifluoroethylene, formula (ii) shown in monomer:
CH
2＝CX
1(CF
2)
nX
2????(ii)
In the formula, X
1Be H or F, X
2Be H, F or Cl, n is at least a kind in 1～10 integer, perfluor (alkyl vinyl ether) class, the propylene.
13. a multilayer body, the layer that it is made of the fluorine-containing adhesive material of claim 1～12 described in each (A), with (B) demonstrate with carbonate group and/or acid halide group by having that layer that the organic materials of affinity or reactive functional group constitutes forms.
14. the multilayer body described in the claim 13, wherein, layer (B) constitutes by have the polymer materials that is selected from a kind of functional group in hydroxyl, carboxyl, carboxylate group, ester group, carboxylic acid ester groups, amino, amide group, imide, sulfydryl, thiolic acid ester group, sulfonic group, Sulfonates, sulfonate group, the epoxy group(ing) in molecular chain at least.
15. the multilayer body described in claim 13 or 14, wherein, layer (B) is made of at the thermoplastic resin below 270 ℃ crystalline melt point or second-order transition temperature.
16. the multilayer body described in the claim 15, wherein, layer (B) is made of at the thermoplastic resin below 230 ℃ crystalline melt point or second-order transition temperature.
17. the multilayer body of claim 13 or 14 described in each, wherein, the polymer materials in layer (B), polyester polyamide-based by being selected from, polycarbonate-based, polyvinyl chloride, polyacrylic, polyvinyl acetate (PVA) class, polyolefins, polyvinyl alcohol, the ethylene-vinyl alcohol copolymer class constitutes.
18. multilayered tube or multi-layer flexible pipe, it is that any multilayer body moulding in the claim 13～17 is formed.
19. multilayer film or multi-layer sheet, it is that any multilayer body moulding in the claim 13～17 is formed.
20. a fuel tank, it is that any multilayer body moulding in the claim 13～17 is formed.
21. a bottle, it is that any multilayer body moulding in the claim 13～17 is formed.
22. a fuel distribution tube is with multilayered tube or fuel distribution tube multi-layer flexible pipe, it be the layer that will constitute by the fluorine-containing adhesive material of claim 1～12 described in each by (A), with (B) demonstrate the multilayer body moulding that the polyamide-based layer that constitutes of organic materials of affinity or reactive functional group forms with carbonate group and/or acid halide group and form by having.
23. a fuel container, the multilayer body moulding that it is the layer that will be made of the fluorine-containing adhesive material of claim 1～12 described in each (A), form with the layer that (B) is made of ethene polymers forms.
24. a soup bottle, the multilayer body moulding that it is the layer that will be made of the fluorine-containing adhesive material of claim 1～12 described in each (A), form with the layer that (B) is made of ethene polymers forms.
25. the manufacture method of a moulded products, it is characterized in that, in the method for making the moulded products described in the claim 18～24, will by have carbonate group and/or acid halide group contain fluorine-containing adhesive material (A) that the vinyl fluoride polymkeric substance constitutes with by having the organic materials (B) that demonstrates affinity or reactive functional group with carbonate group and/or acid halide group, under the temperature that surpasses crystalline melt point separately or second-order transition temperature, adopting simultaneously, extrusion by melting carries out moulding.
26. the manufacture method described in the claim 25, it is characterized in that, with crystalline melt point or second-order transition temperature at the organic materials (B) that fluorine-containing adhesive material (A) that the vinyl fluoride polymkeric substance constitutes and crystalline melt point or second-order transition temperature constitute at the thermoplastic resin below 270 ℃ that contains below 270 ℃, surpassing separately crystalline melt point or second-order transition temperature and under the temperature below 350 ℃, adopting simultaneously, extrusion by melting carries out moulding.
27. the manufacture method described in the claim 25, it is characterized in that, with crystalline melt point or second-order transition temperature at the organic materials (B) that fluorine-containing adhesive material (A) that the vinyl fluoride polymkeric substance constitutes and crystalline melt point or second-order transition temperature constitute at the thermoplastic resin below 230 ℃ that contains below 230 ℃, surpassing separately crystalline melt point or second-order transition temperature and under the temperature below 350 ℃, adopting simultaneously, extrusion by melting carries out moulding.
28. the manufacture method described in the claim 27, wherein, mold temperature is below 300 ℃.
29. a multilayer body, is formed with the layer that (C) is made of inorganic materials the layer that it is made of the fluorine-containing adhesive material of claim 1～12 described in each (A).
30. the multilayer body described in the claim 29, wherein, the inorganic materials of layer (C) is the metal based material.
31. the multilayer body described in the claim 29, wherein, the inorganic materials of layer (C) is the glass based material.
32. the multilayer body of a structure more than 3 layers, wherein, in the multilayer body described in claim 13 or 29, further on layer (A) that side lamination that fluorine-containing adhesive material constitutes by the layer (D) that the vinyl fluoride polymkeric substance constitutes that contains of not carbonate-containing base and/or acid halide group.
33. a fuel distribution tube is with multilayered tube or fuel distribution tube multi-layer flexible pipe, it is that multilayer body moulding with structure more than 3 layers forms, wherein, said more than 3 layers the multilayer body of structure be in the multilayer body described in the claim 22, further on layer (A) that side lamination that fluorine-containing adhesive material constitutes by the layer (D) that the vinyl fluoride polymkeric substance constitutes that contains of not carbonate-containing base and/or acid halide group.
34. a fuel distribution tube is with multilayered tube or fuel distribution tube multi-layer flexible pipe, it is that multilayer body moulding with structure more than 3 layers forms, wherein, said more than 3 layers the multilayer body of structure be in the multilayer body described in the claim 22, further on layer (A) that side lamination that fluorine-containing adhesive material constitutes, have the layer (E) that the vinyl fluoride polymkeric substance constitutes that contains of electroconductibility.
35. a fuel distribution tube is with multilayered tube or fuel distribution tube multi-layer flexible pipe, it is that multilayer body moulding with structure more than 4 layers forms, wherein, said more than 4 layers the multilayer body of structure be in the multilayer body described in the claim 33, further containing the layer (E) that the vinyl fluoride polymkeric substance constitutes that contains that has electroconductibility on layer (D) that side lamination that the vinyl fluoride polymkeric substance constitutes.
36. a fuel distribution tube is with multilayered tube or fuel distribution tube multi-layer flexible pipe; it is that multilayer body moulding with structure more than 3 layers forms; wherein; said more than 3 layers the multilayer body of structure be in the multilayer body of claim 22,33～35 described in each, further protective layer (F) on layer (B) that side lamination of polyamide-based formation.
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP254208/1999 | 1999-09-08 | ||
| JP254208/99 | 1999-09-08 | ||
| JP25420899 | 1999-09-08 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1384861A true CN1384861A (en) | 2002-12-11 |
| CN1183219C CN1183219C (en) | 2005-01-05 |
Family
ID=17261767
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB00815080XA Expired - Lifetime CN1183219C (en) | 1999-09-08 | 2000-09-08 | Fluorochemical adhesive material and layered product obtained with the same |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US6740375B1 (en) |
| EP (1) | EP1245657B1 (en) |
| JP (1) | JP4590812B2 (en) |
| KR (1) | KR100714142B1 (en) |
| CN (1) | CN1183219C (en) |
| AT (1) | ATE344805T1 (en) |
| DE (1) | DE60031797T2 (en) |
| WO (1) | WO2001018142A1 (en) |
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| CN101796435A (en) * | 2007-09-04 | 2010-08-04 | 奥斯兰姆奥普托半导体有限责任公司 | Optical component, method for producing said component, and optoelectronic assembly unit comprising said component |
| CN104070747A (en) * | 2013-03-29 | 2014-10-01 | 杜邦-东丽株式会社 | Protection layer used for high frequency circuit substrate |
| CN109536059A (en) * | 2018-11-08 | 2019-03-29 | 宁波激智科技股份有限公司 | A kind of novel optical protective film |
| CN113677509A (en) * | 2019-04-23 | 2021-11-19 | 株式会社普利司通 | Composite pipe and method for manufacturing composite pipe |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1245657A1 (en) | 2002-10-02 |
| DE60031797D1 (en) | 2006-12-21 |
| JP4590812B2 (en) | 2010-12-01 |
| KR20020035863A (en) | 2002-05-15 |
| ATE344805T1 (en) | 2006-11-15 |
| EP1245657B1 (en) | 2006-11-08 |
| EP1245657A4 (en) | 2004-08-18 |
| US6740375B1 (en) | 2004-05-25 |
| WO2001018142A1 (en) | 2001-03-15 |
| KR100714142B1 (en) | 2007-05-02 |
| DE60031797T2 (en) | 2007-09-06 |
| CN1183219C (en) | 2005-01-05 |
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